HCC provides some software packages via the Apptainer container software. If you do not see a desired package in the module list below, please check the Using Apptainer page for the software list there.
If a module lists one or more prerequisites, the prerequisite module(s) must be loaded before or along with, that module.
For example, the cdo/2.1
modules requires compiler/pgi/13.
To load
the cdo module, doing either
module load compiler/pgi/13
module load cdo/2.1
or
module load compiler/pgi/13 cdo/2.1
(Note the prerequisite module
must be first.)
is acceptable.
Some packages list multiple compilers for prerequisites. This means that the package has been built with each version of the compilers listed.
If you are using custom GPU Anaconda Environment, the only module you need to load is anaconda
:
module load anaconda
last generated 2024-10-11T05:03:34CDT
Name | Version | Module Name | Prerequisites | Type | Domain | Description |
---|---|---|---|---|---|---|
3d-dna | 201008 | 3d-dna/201008 | None | application | computational biology | 3D de novo assembly (3D-DNA) pipeline. |
3dslicer | 4.11.20210226 | 3dslicer/4.11.20210226 | None | application | biomedicine | 3D Slicer is a free, open source and multi-platform software package widely used for medical, biomedical, and related imaging research. |
BICseq | 1.1.2 | BICseq/1.1 | None | application | computational biology | BIC-seq can accurately and efficiently identify CNVs via minimizing the Bayesian information criterion. |
CNVnator | 0.4.1 | CNVnator/0.4 | None | application | genotyping | CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. |
GSL | 2.6 | GSL/2.6 | compiler/pgi/20 compiler/intel/19 compiler/gcc/11 compiler/intel/20 compiler/gcc/10 | library | runtime support | |
LIS | 7.3 | LIS/7.3 | compiler/intel/19:openmpi/4.0 | application | Simulation | |
MEME | 4.11.2 | MEME/4.11 | compiler/gcc/11:openmpi/4.1 | application | computational biology | The MEME suite is a collection of tools for the discovery and analysis of sequence motifs. It is hosted at http://meme-suite.org/. |
MEME | 5.5.5 | MEME/5.5 | compiler/gcc/11:openmpi/4.1 | application | computational biology | The MEME suite is a collection of tools for the discovery and analysis of sequence motifs. It is hosted at http://meme-suite.org/. |
NCL | 6.1 | NCL/6.1 | None | application | utility | NCAR Command Language |
NCL | 6.3 | NCL/6.3 | None | application | utility | NCAR Command Language |
NCL | 6.4 | NCL/6.4 | None | application | utility | NCAR Command Language |
NCL | 6.6.2 | NCL/6.6 | None | application | utility | NCAR Command Language |
NCO | 4.9.4 | NCO/4.9 | compiler/pgi/20 | library | runtime support | |
NCO | 4.9.9 | NCO/4.9 | compiler/intel/20 | library | runtime support | |
NUWRF | v9 | NUWRF/intel/v9 | None | library | runtime support | |
R | 3.4.4 | R/3.4 | None | library | runtime support | R is a free software environment for statistical computing and graphics. |
R | 3.5.1 | R/3.5 | None | library | runtime support | R is a free software environment for statistical computing and graphics. |
R | 3.6.3 | R/3.6 | None | library | runtime support | R is a free software environment for statistical computing and graphics. |
R | 4.0.5 | R/4.0 | None | library | runtime support | R is a free software environment for statistical computing and graphics. |
R | 4.1.3 | R/4.1 | None | library | runtime support | R is a free software environment for statistical computing and graphics. |
R | 4.2.2 | R/4.2 | None | library | runtime support | R is a free software environment for statistical computing and graphics. |
R | 4.3.3 | R/4.3 | None | library | runtime support | R is a free software environment for statistical computing and graphics. |
RAPSearch2 | 2.19 | RAPSearch2/2.19 | None | application | computational biology | RAPSearch2 is a tool for fast protein similarity searches. |
SRAtoolkit | 2.10.0 | SRAtoolkit/2.10 | None | application | computational biology | SRA Toolkit and SDK from NCBI |
SRAtoolkit | 2.11.0 | SRAtoolkit/2.11 | None | application | computational biology | SRA Toolkit and SDK from NCBI |
SRAtoolkit | 2.8.2 | SRAtoolkit/2.8 | None | application | computational biology | SRA Toolkit and SDK from NCBI |
SRAtoolkit | 2.9.6 | SRAtoolkit/2.9 | None | application | computational biology | SRA Toolkit and SDK from NCBI |
StringTie | 1.3.0 | StringTie/1.3 | None | application | computational biology | StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts. |
StringTie | 2.1.2 | StringTie/2.1 | None | application | computational biology | StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts. |
StringTie | 2.2.1 | StringTie/2.2 | None | application | computational biology | StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts. |
TrimGalore | 0.4.5 | TrimGalore/0.4 | None | library | runtime support | |
WRF | v3 | WRF/v3 | compiler/pgi/20:openmpi/4.0 | library | runtime support | |
WRF | v4 | WRF/v4 | compiler/intel/20:openmpi/4.0 compiler/pgi/20:openmpi/4.0 | library | runtime support | |
abacas | 1.3.1 | abacas/1.3 | None | application | computational biology | ABACAS is intended to rapidly contiguate (align, order, orientate), visualize and design primers to close gaps on shotgun assembled contigs based on a reference sequence. |
abaqus | 2021 | abaqus/2021 | None | application | Engineering | Abaqus is a software suite for finite element analysis and computer-aided engineering. |
abayesqr | 1.0 | abayesqr/1.0 | None | application | high-throughput sequencing data | aBayesQR is a viral quasispecies reconstruction algorithm that employs a maximum-likelihood framework to infer individual sequences in a mixture from high-throughput sequencing data. |
abinit | 9.6.2 | abinit/9.6 | compiler/gcc/10:openmpi/4.1 | application | Physics | ABINIT is an atomic-scale simulation software suite. |
abricate | 0.8.13 | abricate/0.8 | None | application | Biology | Mass screening of contigs for antibiotic resistance genes |
abricate | 1.0.1 | abricate/1.0 | None | application | Biology | Mass screening of contigs for antibiotic resistance genes |
adfr-suite | 1.0 | adfr-suite/1.0 | None | application | Chemistry | AutoDockFR (or ADFR in short) is a protein-ligand docking program developed in the Sanner laboratory at Scripps Research under the AutoDock umbrella |
admixtools | 7.0.2 | admixtools/7.0 | None | application | admixture | ADMIXTOOLS (Patterson et al. 2012) is a software package that supports formal tests of whether admixture occurred, and makes it possible to infer admixture proportions and dates. |
afni | 18.2.06 | afni/18.2 | None | application | MRI | AFNI is a suite of programs for looking at and analyzing 3D brain images. |
afni | 21.1.06 | afni/21.1 | None | application | MRI | AFNI is a suite of programs for looking at and analyzing 3D brain images. |
afni | 22.0.21 | afni/22.0 | None | application | MRI | AFNI is a suite of programs for looking at and analyzing 3D brain images. |
afni | 23.1.10 | afni/23.1 | None | application | MRI | AFNI is a suite of programs for looking at and analyzing 3D brain images. |
afq | a42e157 | afq/a42e157 | None | application | matlab toolbox | Automated Fiber Quantification. |
afq | c59f21b | afq/c59f21b | None | application | matlab toolbox | Automated Fiber Quantification. |
afterqc | 0.9.6 | afterqc/0.9 | None | application | package | Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data. AfterQC can simply go through all fastq files in a folder and then output three folders: good, bad and QC folders, which contains good reads, bad reads and the QC results of each fastq file/pair. Currently it supports processing data from HiSeq 2000/2500/3000/4000, Nextseq 500/550, MiniSeq...and other Illumina 1.8 or newer formats. |
agat | 0.9.2 | agat/0.9 | None | application | bioinformatics | Another Gff Analysis Toolkit (AGAT). Suite of tools to handle gene annotations in any GTF/GFF format. |
agfusion | 1.0 | agfusion/1.0 | None | application | Biology | AGFusion is a python package for annotating gene fusions from the human or mouse genomes. |
agfusion | 1.251 | agfusion/1.251 | None | application | Biology | AGFusion is a python package for annotating gene fusions from the human or mouse genomes. |
aligngraph | 1.0 | aligngraph/1.0 | None | application | computational biology | |
allinea | 18.0 | allinea/18.0 | None | application | Utility | |
allinea | 18.2 | allinea/18.2 | None | application | Utility | |
allinea | 19.0 | allinea/19.0 | None | application | Utility | |
allinea | 21.0 | allinea/21.0 | None | application | Utility | |
allinea | 22.0 | allinea/22.0 | None | application | Utility | |
allinea | 22.1 | allinea/22.1 | None | application | Utility | |
allinea | 4.2 | allinea/4.2 | None | application | Utility | |
allinea | 5.0 | allinea/5.0 | None | application | Utility | |
allinea | 5.1 | allinea/5.1 | None | application | Utility | |
allinea | 6.0 | allinea/6.0 | None | application | Utility | |
allinea | 6.1 | allinea/6.1 | None | application | Utility | |
allinea | 7.0 | allinea/7.0 | None | application | Utility | |
ambertools | 22 | ambertools/22 | compiler/gcc/10:openmpi/4.1 | application | computational chemistry | |
ambertools | 23 | ambertools/23 | compiler/gcc/11:openmpi/4.1 compiler/gcc/10:openmpi/4.1 | application | computational chemistry | |
ambertools | 24 | ambertools/24 | compiler/gcc/10:openmpi/4.1 compiler/gcc/11:openmpi/4.1 | application | computational chemistry | |
amorph | 2021.05.10 | amorph/2021.05.10 | None | application | environment | AMORPH utilizes a new Bayesian statistical approach to interpreting X-ray diffraction results of samples with both crystalline and amorphous components. |
amos | 3.1.0 | amos/3.1 | None | application | computational biology | A Modular, Open-Source whole genome assembler |
anaconda | 2.7 | anaconda/2.7 | None | application | system | |
anaconda | 23.1.0/1.3.1 | anaconda/23.1 | None | application | system | |
anaconda | 23.11.0/1.5.4 | anaconda/23.11 | None | application | system | |
anaconda | 23.7.2/1.4.9 | anaconda/23.7 | None | application | system | |
anaconda | 3.3 | anaconda/3.3 | None | application | system | |
anaconda | 3.4 | anaconda/3.4 | None | application | system | |
anaconda | 4.10.3 | anaconda/4.10 | None | application | system | |
anaconda | 4.12.0/0.24.0 | anaconda/4.12 | None | application | system | |
anaconda | 4.3 | anaconda/4.3 | None | application | system | |
anaconda | 4.6 | anaconda/4.6 | None | application | system | |
anaconda | 4.8 | anaconda/4.8 | None | application | system | |
anaconda | 4.9.2 | anaconda/4.9 | None | application | system | |
angsd | 0.935 | angsd/0.935 | None | application | Bioinformatics | ANGSD: Analysis of next generation Sequencing Data |
angsd | 0.937 | angsd/0.937 | None | application | Bioinformatics | ANGSD: Analysis of next generation Sequencing Data |
ansys | 19.2 | ansys/19.2 | None | application | Engineering | ANSYS offers a comprehensive software suite that spans the entire range of physics, providing access to virtually any field of engineering simulation that a design process requires. |
ansys | 2021R2 | ansys/2021 | None | application | Engineering | ANSYS offers a comprehensive software suite that spans the entire range of physics, providing access to virtually any field of engineering simulation that a design process requires. |
ant | 1.10.1 | ant/1.10 | None | library | java | Java build tool |
ant | 1.9.9 | ant/1.9 | None | library | java | Java build tool |
antismash | 6.1.0 | antismash/6.1 | None | application | Biology | antiSMASH - the antibiotics and Secondary Metabolite Analysis SHell |
ants | 2.5.1 | ants/2.5 | None | application | computational neuroimaging | ANTs computes high-dimensional mappings to capture the statistics of brain structure and function. |
anvio | 6.1 | anvio/6.1 | None | application | Omics | A platform for integrated multi-omics |
anvio | 6.2 | anvio/6.2 | None | application | Omics | A platform for integrated multi-omics |
anvio | 7 | anvio/7 | None | application | Omics | A platform for integrated multi-omics |
anvio | 7.1 | anvio/7.1 | None | application | Omics | A platform for integrated multi-omics |
apkid | 1.0.0 | apkid/1.0 | None | application | Malware | APKiD is Android Application Identifier for Packers, Protectors, Obfuscators and Oddities - PEiD for Android. |
apptainer | 1.1 | apptainer/1.1 | None | application | system | Application containers enabling mobility of compute. |
aria2 | 1.23.0 | aria2/1.23 | None | application | tool | aria2 is a lightweight multi-protocol & multi-source command-line download utility. |
aria2 | 1.34.0 | aria2/1.34 | None | application | tool | aria2 is a lightweight multi-protocol & multi-source command-line download utility. |
aria2 | 1.36.0 | aria2/1.36 | None | application | tool | aria2 is a lightweight multi-protocol & multi-source command-line download utility. |
aria2 | 1.37.0 | aria2/1.37 | None | application | tool | aria2 is a lightweight multi-protocol & multi-source command-line download utility. |
arpack-ng | 3.9.1 | arpack-ng/3.9 | compiler/intel/20:openmpi/4.1 | library | runtime support | |
arriba | 2.4.0 | arriba/2.4 | None | application | computational biology | Fast and accurate gene fusion detection from RNA-Seq data |
art | 2.6.0 | art/2.6 | None | application | computational biology | ART is a set of simulation tools to generate synthetic next-generation sequencing reads. |
ase | 3.18.1 | ase/3.18 | None | application | Physics | ASE is a python package providing an open source Atomic Simulation Environment in the Python language. |
ashs | 1.0.0 | ashs/1.0 | None | application | MRI | ASHS is software for automatic segmentation of the medial temporal lobe (MTL) substructures from brain MRI scans. |
ashs | 2.0.0 | ashs/2.0 | None | application | MRI | ASHS is software for automatic segmentation of the medial temporal lobe (MTL) substructures from brain MRI scans. |
aspera-cli | 3.7.7 | aspera-cli/3.7 | None | application | system | IBM Aspera Command-Line Interface (the Aspera CLI) is a collection of Aspera tools for performing high-speed, secure data transfers from the command line. |
aspera-cli | 4.14.0 | aspera-cli/4.14 | None | application | system | IBM Aspera Command-Line Interface (the Aspera CLI) is a collection of Aspera tools for performing high-speed, secure data transfers from the command line. |
asreml | 3.0 | asreml/3.0 | None | application | data analysis | ASReml |
asreml | 4.1 | asreml/4.1 | None | application | data analysis | ASReml |
asreml | 4.2 | asreml/4.2 | None | application | data analysis | ASReml |
atat | 3.36 | atat/3.36 | compiler/gcc/11 | application | Chemistry | |
atk | 2016.3 | atk/2016.3 | None | application | Chemistry | |
atomate2 | 0.0.10 | atomate2/py38/0.0.10 | None | application | Simulation | atomate2 is a library of materials science workflows |
atomate2 | 0.0.10 | atomate2/py39/0.0.10 | None | application | Simulation | atomate2 is a library of materials science workflows |
atomate2 | 0.0.10 | atomate2/py310/0.0.10 | None | application | Simulation | atomate2 is a library of materials science workflows |
augur | 12.0.0 | augur/12.0 | None | application | public health | Process pathogen genome data for the Nextstrain platform |
augustus | 3.0 | augustus/3.0 | None | application | computational biology | AUGUSTUS is a gene prediction program for eukaryotes written by Mario Stanke and Oliver Keller. It can be used as an ab initio program, which means it bases its prediction purely on the sequence. AUGUSTUS may also incorporate hints on the gene structure coming from extrinsic sources such as EST, MS/MS, protein alignments and synthenic genomic alignments. |
augustus | 3.2.3 | augustus/3.2 | None | application | computational biology | AUGUSTUS is a gene prediction program for eukaryotes written by Mario Stanke and Oliver Keller. It can be used as an ab initio program, which means it bases its prediction purely on the sequence. AUGUSTUS may also incorporate hints on the gene structure coming from extrinsic sources such as EST, MS/MS, protein alignments and synthenic genomic alignments. |
augustus | 3.3 | augustus/3.3 | None | application | computational biology | AUGUSTUS is a gene prediction program for eukaryotes written by Mario Stanke and Oliver Keller. It can be used as an ab initio program, which means it bases its prediction purely on the sequence. AUGUSTUS may also incorporate hints on the gene structure coming from extrinsic sources such as EST, MS/MS, protein alignments and synthenic genomic alignments. |
augustus | 3.4 | augustus/3.4 | None | application | computational biology | AUGUSTUS is a gene prediction program for eukaryotes written by Mario Stanke and Oliver Keller. It can be used as an ab initio program, which means it bases its prediction purely on the sequence. AUGUSTUS may also incorporate hints on the gene structure coming from extrinsic sources such as EST, MS/MS, protein alignments and synthenic genomic alignments. |
augustus | 3.5.0 | augustus/3.5 | None | application | computational biology | AUGUSTUS is a gene prediction program for eukaryotes written by Mario Stanke and Oliver Keller. It can be used as an ab initio program, which means it bases its prediction purely on the sequence. AUGUSTUS may also incorporate hints on the gene structure coming from extrinsic sources such as EST, MS/MS, protein alignments and synthenic genomic alignments. |
autoconf | 1.0 | autoconf/2.69 | None | application | Utilities | The autotools collection is a set of tools that make it easy to build and install programs from a source distribution. |
autodock | 4.2.6 | autodock/4.2 | None | application | Chemistry | AutoDock is a suite of automated docking tools. It is designed to predict how small molecules, such as substrates or drug candidates, bind to a receptor of known 3D structure. |
autodock-gpu | 1.2 | autodock-gpu/1.2 | None | application | Chemistry | AutoDock for GPUs using CUDA. |
autodock-gpu | 1.3 | autodock-gpu/1.3 | None | application | Chemistry | AutoDock for GPUs using CUDA. |
autodock-gpu | 1.4.3 | autodock-gpu/1.4 | None | application | Chemistry | AutoDock for GPUs using CUDA. |
autodock-gpu | 1.5.3 | autodock-gpu/1.5 | None | application | Chemistry | AutoDock for GPUs using CUDA. |
autodock-gpu | 2024.03.05 | autodock-gpu/2024.03.05 | None | application | Chemistry | AutoDock for GPUs using CUDA. |
autodock-gpu | 4.2.6.c135512 | autodock-gpu/4.2 | None | application | Chemistry | AutoDock for GPUs using CUDA. |
autodock-vina | 1.1.2 | autodock-vina/1.1 | None | application | Chemistry | AutoDock Vina is an open-source program for doing molecular docking |
automake | 1.0 | automake/1.16 | None | application | Utilities | The autotools collection is a set of tools that make it easy to build and install programs from a source distribution. |
autotools | 1.0 | autotools/1.0 | None | application | Utilities | The autotools collection is a set of tools that make it easy to build and install programs from a source distribution. |
awscli | 1.1.120 | awscli/1.11 | None | application | utility | Universal Command Line Environment for AWS. |
awscli | 1.19.5 | awscli/1.19 | None | application | utility | Universal Command Line Environment for AWS. |
awscli | 1.23.6 | awscli/1.23 | None | application | utility | Universal Command Line Environment for AWS. |
azcopy | 7.2.0 | azcopy/7.2 | None | application | Utility | AzCopy is a command-line utility designed for copying data to/from Microsoft Azure Blob and File storage, using simple commands designed for optimal performance. |
ballgown | 2.2.0 | ballgown/2.2 | None | application | computational biology | Ballgown is a software package designed to facilitate flexible differential expression analysis of RNA-Seq data. It also provides functions to organize, visualize, and analyze the expression measurements for your transcriptome assembly. |
bam-readcount | 0.6 | bam-readcount/0.6 | None | application | computational biology | The purpose of this program is to generate metrics at single nucleotide positions. |
bam-readcount | 0.8 | bam-readcount/0.8 | None | application | computational biology | The purpose of this program is to generate metrics at single nucleotide positions. |
bamm | 1.7.3 | bamm/1.7 | None | application | computational biology | Metagenomics-focused BAM file manipulation |
bamscale | 0.0.5 | bamscale/0.0.5 | None | application | computational biology | BAMscale is a one-step tool for either 1) quantifying and normalizing the coverage of peaks |
bamtools | 2.3.0 | bamtools/2.3 | None | application | computational biology | C++ API & command-line toolkit for working with BAM data |
bamtools | 2.4.1 | bamtools/2.4 | None | application | computational biology | C++ API & command-line toolkit for working with BAM data |
bamtools | 2.5.1 | bamtools/2.5 | None | application | computational biology | C++ API & command-line toolkit for working with BAM data |
basespace-cli | 1.1.0 | basespace-cli/1.1 | None | application | biology | Toolkit to perform regulatory genomics data analysis |
basetools/gapfiller | 1.10 | basetools/gapfiller/1.10 | None | application | computational biology | GapFiller is a stand-alone program for closing gaps within pre-assembled scaffolds. |
basetools/sspace-standard | 3.0 | basetools/sspace-standard/3.0 | None | application | computational biology | SSPACE-standard is a stand-alone program for scaffolding pre-assembled contigs using NGS paired-read data. |
bayespeak | 1.24.0 | bayespeak/1.24.0 | None | application | computational biology | This package is an implementation of the BayesPeak algorithm for peak-calling in ChIP-seq data. |
bbmap | 37.17 | bbmap/37.17 | None | application | computational biology | BBMap is a splice-aware global aligner for DNA and RNA sequencing reads. |
bbmap | 38.06 | bbmap/38.06 | None | application | computational biology | BBMap is a splice-aware global aligner for DNA and RNA sequencing reads. |
bbmap | 38.84 | bbmap/38.84 | None | application | computational biology | BBMap is a splice-aware global aligner for DNA and RNA sequencing reads. |
bbmap | 39.06 | bbmap/39.06 | None | application | computational biology | BBMap is a splice-aware global aligner for DNA and RNA sequencing reads. |
bc | 1.07.1 | bc/1.07 | None | application | Utility | bc is an arbitrary precision numeric processing language. |
bcftools | 1.10.2 | bcftools/1.10 | None | application | computational biology | BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed. Most commands accept VCF, bgzipped VCF and BCF with filetype detected automatically even when streaming from a pipe. Indexed VCF and BCF will work in all situations. Un-indexed VCF and BCF and streams will work in most, but not all situations. |
bcftools | 1.17 | bcftools/1.17 | None | application | computational biology | BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed. Most commands accept VCF, bgzipped VCF and BCF with filetype detected automatically even when streaming from a pipe. Indexed VCF and BCF will work in all situations. Un-indexed VCF and BCF and streams will work in most, but not all situations. |
bcftools | 1.2 | bcftools/1.2 | None | application | computational biology | BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed. Most commands accept VCF, bgzipped VCF and BCF with filetype detected automatically even when streaming from a pipe. Indexed VCF and BCF will work in all situations. Un-indexed VCF and BCF and streams will work in most, but not all situations. |
bcftools | 1.3.1 | bcftools/1.3 | None | application | computational biology | BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed. Most commands accept VCF, bgzipped VCF and BCF with filetype detected automatically even when streaming from a pipe. Indexed VCF and BCF will work in all situations. Un-indexed VCF and BCF and streams will work in most, but not all situations. |
bcftools | 1.8 | bcftools/1.8 | None | application | computational biology | BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed. Most commands accept VCF, bgzipped VCF and BCF with filetype detected automatically even when streaming from a pipe. Indexed VCF and BCF will work in all situations. Un-indexed VCF and BCF and streams will work in most, but not all situations. |
bcftools | 1.9 | bcftools/1.9 | None | application | computational biology | BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed. Most commands accept VCF, bgzipped VCF and BCF with filetype detected automatically even when streaming from a pipe. Indexed VCF and BCF will work in all situations. Un-indexed VCF and BCF and streams will work in most, but not all situations. |
bcl2fastq | 1.8.4 | bcl2fastq/1.8 | None | application | biology | bcl2fastq can be used to demultiplex data and convert BCL files to FASTQ file formats for downstream analysis |
bcl2fastq2 | 2.20.0.422 | bcl2fastq2/2.20 | None | application | computational biology | The Illumina bcl2fastq2 Conversion Software v2.20 demultiplexes sequencing data and converts base call (BCL) files into FASTQ files. |
beagle | 4.1_21Jan17.6cc | beagle/4.1 | None | application | Biology | Beagle is a software package that performs genotype calling, genotype phasing, imputation of ungenotyped markers, and identity-by-descent segment detection. |
beagle | 5.1_24Aug19.3e8 | beagle/5.1 | None | application | Biology | Beagle is a software package that performs genotype calling, genotype phasing, imputation of ungenotyped markers, and identity-by-descent segment detection. |
beagle | 5.2_21Apr21.304 | beagle/5.2 | None | application | Biology | Beagle is a software package that performs genotype calling, genotype phasing, imputation of ungenotyped markers, and identity-by-descent segment detection. |
beagle-lib | 4.0.0 | beagle-lib/4.0 | None | application | computational biology | general purpose library for evaluating the likelihood of sequence evolution on trees |
beast | 1.10 | beast/1.10 | None | application | biology | BEAST is a cross-platform program for Bayesian analysis of molecular sequences using MCMC. |
beast | 1.8 | beast/1.8 | None | application | biology | BEAST is a cross-platform program for Bayesian analysis of molecular sequences using MCMC. |
beast2 | 2.4 | beast2/2.4 | None | application | biology | BEAST 2 is a cross-platform program for Bayesian phylogenetic analysis of molecular sequences. |
beast2 | 2.6.3 | beast2/2.6 | None | application | biology | BEAST 2 is a cross-platform program for Bayesian phylogenetic analysis of molecular sequences. |
beast2 | 2.7.5 | beast2/2.7 | None | application | biology | BEAST 2 is a cross-platform program for Bayesian phylogenetic analysis of molecular sequences. |
bedops | 2.4.35 | bedops/2.4 | None | application | computational biology | BEDOPS is an open-source command-line toolkit that performs highly efficient and scalable Boolean and other set operations, statistical calculations, archiving, conversion and other management of genomic data of arbitrary scale. |
bedtools | 2.24.0 | bedtools/2.24 | None | application | computational biology | A powerful toolset for genome arithmetic |
bedtools | 2.27.1 | bedtools/2.27 | None | application | computational biology | A powerful toolset for genome arithmetic |
bertopic | 0.13.0 | bertopic/0.13 | None | application | Modeling | BERTopic performs topic Modeling with state-of-the-art transformer models. |
beta | 1.0.7 | beta/1.0 | None | application | computational biology | Binding and Expression Target Analysis (BETA) is a software package that integrates ChIP-seq of transcription factors or chromatin regulators with differential gene expression data to infer direct target genes. |
bfc | r181 | bfc/r181 | None | application | Biology | BFC is a standalone high-performance tool for correcting sequencing errors from Illumina sequencing data. |
bicseq2-norm | 0.2.4 | bicseq2-norm/0.2 | None | application | bioinformatics | BICseq2-norm is for normalizing potential biases in the sequencing data. |
bicseq2-seg | 0.7.2 | bicseq2-seg/0.7 | None | application | bioinformatics | BICseq2-seg is for detecting CNVs based on the normalized data given by BICseq2-norm. |
bidscoin | 4.0.0 | bidscoin/py38/4.0 | None | application | neuroimaging | Converts and organises raw MRI data-sets according to the Brain Imaging Data Structure (BIDS). |
binutils | 2.30 | binutils/2.30 | None | application | Utilities | The GNU Binutils are a collection of binary tools. |
binutils | 2.35.1 | binutils/2.35 | None | application | Utilities | The GNU Binutils are a collection of binary tools. |
binutils | 2.38 | binutils/2.38 | None | application | Utilities | The GNU Binutils are a collection of binary tools. |
bioawk | 1.0 | bioawk/1.0 | None | application | Biology | BWK awk modified for biological data |
biobambam | 2.0.183 | biobambam/2.0 | None | application | computational biology | Tools for early stage alignment file processing |
bioconductor | 3.11 | bioconductor/4.0 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.13 | bioconductor/r41/3.13 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.14 | bioconductor/r41/3.14 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.16 | bioconductor/r42/3.16 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.17 | bioconductor/r43/3.17 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.18 | bioconductor/r43/3.18 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.4 | bioconductor/r34/3.6 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.6 | bioconductor/3.4 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.8 | bioconductor/r35/3.8 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 3.8 | bioconductor/3.8 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor | 4.0 | bioconductor/r40/3.11 | None | application | computational biology | Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data. |
bioconductor-ballgown | 2.2.0 | bioconductor-ballgown/2.2 | None | application | computational biology | Tools for statistical analysis of assembled transcriptomes, including flexible differential expression analysis, visualization of transcript structures, and matching of assembled transcripts to annotation. |
bioconductor-jmosaics | 1.10 | bioconductor-jmosaics/1.10 | None | application | computational biology | Joint analysis of multiple ChIP-Seq data sets. |
biodata | 1.0 | biodata/1.0 | None | application | computational biology | Static data resources for bioinformatics/computational biology. |
biom-format | 2.1.10 | biom-format/2.1 | None | application | computational biology | The BIOM file format (canonically pronounced biome) is designed to be a general-use format for representing biological sample by observation contingency tables. BIOM is a recognized standard for the Earth Microbiome Project and is a Genomics Standards Consortium supported project. |
bioperl | 1.6.924 | bioperl/1.6 | None | application | computational biology | BioPerl is a collection of Perl modules that facilitate the development of Perl scripts for bioinformatics applications. |
bioperl | 1.7.8 | bioperl/1.7 | None | application | computational biology | BioPerl is a collection of Perl modules that facilitate the development of Perl scripts for bioinformatics applications. |
biopython | 1.70 | biopython/py27/1.70 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.70 | biopython/py35/1.70 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.70 | biopython/py36/1.70 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.71 | biopython/py27/1.71 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.71 | biopython/py35/1.71 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.71 | biopython/py36/1.71 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.74 | biopython/py27/1.74 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.74 | biopython/py37/1.74 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.76 | biopython/py27/1.76 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.76 | biopython/py37/1.76 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.77 | biopython/py37/1.77 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.77 | biopython/py38/1.77 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.79 | biopython/py36/1.79 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.79 | biopython/py37/1.79 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.79 | biopython/py38/1.79 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.79 | biopython/py39/1.79 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.81 | biopython/py39/1.81 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.81 | biopython/py310/1.81 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biopython | 1.81 | biopython/py311/1.81 | None | application | biological computation | Collection of freely available tools for computational molecular biology |
biosamtools | 1.38 | biosamtools/1.38 | None | application | computational biology | |
biser | 1.4 | biser/1.4 | None | application | computational biology | Fast Characterization of Segmental Duplication Structure in Multiple Genome Assemblies. |
bismark | 0.14.2 | bismark/0.14 | None | application | computational biology | Bismark is a program to map bisulfite treated sequencing reads to a genome of interest and perform methylation calls in a single step. |
bismark | 0.19.1 | bismark/0.19 | None | application | computational biology | Bismark is a program to map bisulfite treated sequencing reads to a genome of interest and perform methylation calls in a single step. |
bismark | 0.24.1 | bismark/0.24 | None | application | computational biology | Bismark is a program to map bisulfite treated sequencing reads to a genome of interest and perform methylation calls in a single step. |
bison | 3.7.5 | bison/3.7 | None | application | Utility | General purpose parser generator converting annotated context-free grammar to a deterministic LR/GLR parser. |
blast | 2.10.0 | blast/2.10 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.12.0 | blast/2.12 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.13.0 | blast/2.13 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.14.0 | blast/2.14 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.15.0 | blast/2.15 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.2.29 | blast/2.2.29 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.2.30 | blast/2.2 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.4.0 | blast/2.4 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.6.0 | blast/2.6 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast | 2.7.1 | blast/2.7 | None | application | computational biology | NCBI BLAST+ sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blast-legacy | 2.2.26 | blast-legacy/2.2.26 | None | application | computational biology | NCBI BLAST sequence alignment package. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. |
blat | 35 | blat/35x1 | None | application | computational biology | BLAT is a bioinformatics software tool which performs rapid mRNA/DNA and cross-species protein alignments. |
blat | 35 | blat/35 | None | application | computational biology | BLAT is a bioinformatics software tool which performs rapid mRNA/DNA and cross-species protein alignments. |
blat | 36 | blat/36 | None | application | computational biology | BLAT is a bioinformatics software tool which performs rapid mRNA/DNA and cross-species protein alignments. |
blender | 4.2.0 | blender/4.2 | None | application | 3D | Blender is a free and open-source 3D computer graphics software tool set. |
blobtoolkit | 4.1.4 | blobtoolkit/py39/4.1 | None | application | bioinformatics | Interactive quality assessment of genome assemblies. |
blobtoolkit | 4.1.4 | blobtoolkit/py310/4.1 | None | application | bioinformatics | Interactive quality assessment of genome assemblies. |
blobtools | 1.1.1 | blobtools/1.1 | None | application | Bioinformatics | Modular command-line solution for visualisation, quality control and taxonomic partitioning of genome datasets |
boa-bacfinder | 0.0.2016.02.11 | boa-bacfinder/2016.02.11 | None | application | computational biology | Find bacteriocins in bacterial genomes |
boost | 1.44 | boost/1.44 | None | application | System Environment/Base | Boost provides free peer-reviewed portable C++ source libraries. |
boost | 1.55.0 | boost/1.55.0 | None | application | System Environment/Base | Boost provides free peer-reviewed portable C++ source libraries. |
boost | 1.66 | boost/1.66 | compiler/gcc/10 compiler/gcc/9 | application | System Environment/Base | Boost provides free peer-reviewed portable C++ source libraries. |
boost | 1.69 | boost/1.69 | compiler/gcc/9 | application | System Environment/Base | Boost provides free peer-reviewed portable C++ source libraries. |
boost | 1.75 | boost/1.75 | compiler/gcc/9 compiler/intel/18 compiler/intel/20 compiler/gcc/10 compiler/gcc/11 compiler/intel/2021 compiler/intel/19 | application | System Environment/Base | Boost provides free peer-reviewed portable C++ source libraries. |
boris2 | 3.0 | boris2/3.0 | None | application | Physics | Boris Computational Spintronics. |
bowtie | 1.0 | bowtie/1.0 | None | application | computational biology | Fast and sensitive read alignment |
bowtie | 1.1.2 | bowtie/1.1 | None | application | computational biology | Fast and sensitive read alignment |
bowtie | 1.3.1 | bowtie/1.3 | None | application | computational biology | Fast and sensitive read alignment |
bowtie | 2.2.8 | bowtie/2.2 | None | application | computational biology | Fast and sensitive read alignment |
bowtie | 2.3.5 | bowtie/2.3 | None | application | computational biology | Fast and sensitive read alignment |
bowtie | 2.4.4 | bowtie/2.4 | None | application | computational biology | Fast and sensitive read alignment |
bowtie | 2.5.1 | bowtie/2.5 | None | application | computational biology | Fast and sensitive read alignment |
boxnotes2html | 0.1.4 | boxnotes2html/0.1 | None | application | Utility | Converting from Box Notes to HTML or other formats |
bracken | 2.6.0 | bracken/2.6 | None | application | bioinformatics | Bracken (Bayesian Reestimation of Abundance with KrakEN) is a highly accurate statistical method that computes the abundance of species in DNA sequences from a metagenomics sample. |
braker2 | 2.1.2 | braker2/2.1 | None | application | computational biology | BRAKER2 is an extension of BRAKER1 which allows for fully automated training of the gene prediction tools GeneMark-EX and AUGUSTUS from RNA-Seq and/or protein homology information, and that integrates the extrinsic evidence from RNA-Seq and protein homology information into the prediction. |
breakdancer | 1.4 | breakdancer/1.4 | None | application | computational biology | BreakDancer is a Perl/C++ package that provides genome-wide detection of structural variants from next generation paired-end sequencing reads. |
breakseq2 | 2.2 | breakseq2/2.2 | None | application | computational biology | BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants. |
bsmap | 2.90 | bsmap/2.90 | None | application | Mapping | BSMAP is a short reads mapping software for bisulfite sequencing reads. |
busco | 3.0.2 | busco/py27/3.0 | None | application | computational biology | BUSCO provides measures for quantitative assessment of genome assembly, gene set, and transcriptome completeness based on evolutionarily informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB. |
busco | 3.0.2 | busco/py35/3.0 | None | application | computational biology | BUSCO provides measures for quantitative assessment of genome assembly, gene set, and transcriptome completeness based on evolutionarily informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB. |
busco | 3.0.2 | busco/py36/3.0 | None | application | computational biology | BUSCO provides measures for quantitative assessment of genome assembly, gene set, and transcriptome completeness based on evolutionarily informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB. |
busco | 4.0.6 | busco/py36/4.0 | None | application | computational biology | BUSCO provides measures for quantitative assessment of genome assembly, gene set, and transcriptome completeness based on evolutionarily informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB. |
busco | 5.4.3 | busco/py39/5.4 | None | application | computational biology | BUSCO provides measures for quantitative assessment of genome assembly, gene set, and transcriptome completeness based on evolutionarily informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB. |
bwa | 0.6.2 | bwa/0.6 | None | application | computational biology | Burrow-Wheeler Aligner for short-read alignment. |
bwa | 0.7.17 | bwa/0.7 | None | application | computational biology | Burrow-Wheeler Aligner for short-read alignment. |
bwa-mem2 | 2.2.1 | bwa-mem2/2.2 | None | application | computational biology | The next version of bwa-mem. |
bx-python | 0.8.1 | bx-python/py27/0.8 | None | application | computational biology | Tools for manipulating biological data, particularly multiple sequence alignments |
bx-python | 0.8.1 | bx-python/py35/0.8 | None | application | computational biology | Tools for manipulating biological data, particularly multiple sequence alignments |
bx-python | 0.8.1 | bx-python/py36/0.8 | None | application | computational biology | Tools for manipulating biological data, particularly multiple sequence alignments |
bzip2 | 1.0 | bzip2/1.0 | compiler/gcc/10 compiler/intel/18 None compiler/gcc/11 compiler/intel/19 compiler/gcc/9 compiler/intel/20 | library | runtime support | |
bzip2 | 1.0.8 | bzip2/1.0 | compiler/pgi/20 | library | runtime support | |
caffe | 1.0 | caffe/1.0 | None | application | package | It is developed by the Berkeley Vision and Learning Center (BVLC) and by community contributors. Yangqing Jia created the project during his PhD at UC Berkeley. Caffe is released under the BSD 2-Clause license. |
caffe-gpu | 1.0 | caffe-gpu/1.0 | None | application | package | It is developed by the Berkeley Vision and Learning Center (BVLC) and by community contributors. Yangqing Jia created the project during his PhD at UC Berkeley. Caffe is released under the BSD 2-Clause license. |
cairo | 1.16.0 | cairo/1.16 | compiler/intel/20 compiler/pgi/20 | library | runtime support | |
canu | 1.7 | canu/1.7 | None | application | computational biology | Canu is a fork of the Celera Assembler, designed for high-noise single-molecule sequencing (such as the PacBio RS II/Sequel or Oxford Nanopore MinION). |
canu | 1.8 | canu/1.8 | None | application | computational biology | Canu is a fork of the Celera Assembler, designed for high-noise single-molecule sequencing (such as the PacBio RS II/Sequel or Oxford Nanopore MinION). |
canu | 2.1.1 | canu/2.1 | None | application | computational biology | Canu is a fork of the Celera Assembler, designed for high-noise single-molecule sequencing (such as the PacBio RS II/Sequel or Oxford Nanopore MinION). |
canu | 2.2 | canu/2.2 | None | application | computational biology | Canu is a fork of the Celera Assembler, designed for high-noise single-molecule sequencing (such as the PacBio RS II/Sequel or Oxford Nanopore MinION). |
cap3 | 122107 | cap3/122107 | None | application | computational biology | CAP3: A DNA Sequence Assembly Program |
carlsim | 3.1 | carlsim/3.1 | None | application | computational biology | CARLsim is an efficient, easy-to-use, GPU-accelerated software framework for simulating large-scale spiking neural network (SNN) models with a high degree of biological detail. |
carlsim | 4.0 | carlsim/4.0 | None | application | computational biology | CARLsim is an efficient, easy-to-use, GPU-accelerated software framework for simulating large-scale spiking neural network (SNN) models with a high degree of biological detail. |
carnac-lr | 1.0.0 | carnac-lr/1.0 | None | application | computational biology | Clustering coefficient-based Acquisition of RNA Communities in Long Read |
carveme | 1.5.1 | carveme/1.5 | None | application | genomics | CarveMe is a python-based tool for genome-scale metabolic model reconstruction. |
cas-offinder | 2.4 | cas-offinder/2.4 | None | application | Biology | Cas-OFFinder is OpenCL based, ultrafast and versatile program that searches for potential off-target sites of CRISPR/Cas-derived RNA-guided endonucleases (RGEN). |
cblaster | 1.3.11 | cblaster/1.3 | None | application | computational biology | Find clustered hits from a BLAST search. |
ccat | 3.0 | ccat/3.0 | None | application | computational biology | A software package for the analysis of ChIP-seq data with negative control. |
ccp4 | 7.0 | ccp4/7.0 | None | unknown | unknown | |
cd-hit | 4.8.1 | cd-hit/4.8 | None | application | Bioinformatics | CD-HIT is a very widely used program for clustering and comparing protein or nucleotide sequences. |
cd-hit-auxtools | 4.6.8 | cd-hit-auxtools/4.6 | None | application | Bioinformatics | CD-HIT is a very widely used program for clustering and comparing protein or nucleotide sequences. This module specifically loads the auxillary tools. |
cdna-cupcake-tofu2 | 5.2 | cdna-cupcake-tofu2/5.2 | None | application | computational biology | cDNA_Cupcake is a miscellaneous collection of Python and R scripts used for analyzing sequencing data. |
cdo | 1.9.7.1 | cdo/1.9 | None | application | Utilities | CLI tools to manipulate and analyse Climate and NWP model Data |
cdo | 2.4.0 | cdo/2.4 | None | application | Utilities | CLI tools to manipulate and analyse Climate and NWP model Data |
cdsapi | 0.6.1 | cdsapi/py39/0.6 | None | application | Copernicus Climate Data Store | API to access the Copernicus Climate Data Store at ECMWF |
cdsapi | 0.6.1 | cdsapi/py310/0.6 | None | application | Copernicus Climate Data Store | API to access the Copernicus Climate Data Store at ECMWF |
cdsapi | 0.6.1 | cdsapi/py311/0.6 | None | application | Copernicus Climate Data Store | API to access the Copernicus Climate Data Store at ECMWF |
cdsapi | 0.7.2 | cdsapi/py310/0.7 | None | application | Copernicus Climate Data Store | API to access the Copernicus Climate Data Store at ECMWF |
cdsapi | 0.7.2 | cdsapi/py312/0.7 | None | application | Copernicus Climate Data Store | API to access the Copernicus Climate Data Store at ECMWF |
cellranger | 3.0.2 | cellranger/3.0 | None | application | computational biology | Cell Ranger is a set of analysis pipelines that process Chromium single-cell RNA-seq output to align reads, generate feature-barcode matrices and perform clustering and gene expression analysis. |
cenote-taker2 | 2.1.2 | cenote-taker2/2.1 | None | application | computational biology | Cenote-Taker2 is a pipeline for divergent virus discovery and annotation. |
cenote-taker2 | 2020.04.01 | cenote-taker2/2020.04.01 | None | application | computational biology | Cenote-Taker2 is a pipeline for divergent virus discovery and annotation. |
cexor | 1.10 | cexor/1.10 | None | application | computational biology | An R package to uncover high-resolution protein-DNA interactions in ChIP-exo replicates. |
cgmaptools | 0.1.2 | cgmaptools/0.1 | None | application | computational biology | Command-line Toolset for Bisulfite Sequencing Data Analysis |
checkm-genome | 1.0.18 | checkm-genome/1.0 | None | application | computational biology | Assess the quality of microbial genomes recovered from isolates, single cells, and metagenomes. |
checkm-genome | 1.1.2 | checkm-genome/1.1 | None | application | computational biology | Assess the quality of microbial genomes recovered from isolates, single cells, and metagenomes. |
checkm2 | 1.0.1 | checkm2/1.0 | None | application | bioinformatics | CheckM2 - Predicting the quality of metagenome-recovered bins |
checkv | 0.7.0 | checkv/0.7 | None | application | Biology | Assess the quality of metagenome-assembled viral genomes. |
checkv | 0.8.1 | checkv/0.8 | None | application | Biology | Assess the quality of metagenome-assembled viral genomes. |
chemdata | 1.0 | chemdata/1.0 | None | application | computational chemistry | Static data resources for computational chemistry (docking, etc.). |
chewbbaca | 2.8.4 | chewbbaca/2.8 | None | application | computational biology | A complete suite for gene-by-gene schema creation and strain identification. |
chromosomer | 0.1.4a | chromosomer/0.1.4a | None | application | Bioinformatics | A reference-assisted assembly tool for producing draft chromosome sequences. |
circlator | 1.5.5 | circlator/1.5 | None | application | Biology | circlator: a tool to circularise genome assemblies |
circleator | 1.0.2 | circleator/1.0 | None | application | computational biology | Flexible circular visualization of genome-associated data with BioPerl and SVG. |
cite-seq-count | 1.4.4 | cite-seq-count/1.4 | None | application | Bioinformatics | A python package to map reads from CITE-seq or hashing data for single cell experiments |
clark | 1.2 | clark/1.2 | None | application | computational biology | |
clearcut | 1.0 | clearcut/1.0 | None | application | computational biology | Clearcut - The reference implementation for Relaxed Neighbor Joining (RNJ) |
clove | 0.17 | clove/0.17 | None | application | computational biology | CLOVE: Classification of genomic fusions into structural variation events. |
clustal-omega | 1.2 | clustal-omega/1.2 | None | application | computational biology | Clustal Omega is the latest addition to the Clustal family. It offers a significant increase in scalability over previous versions, allowing hundreds of thousands of sequences to be aligned in only a few hours |
clustalw | 2.1 | clustalw/2.1 | None | application | computational biology | ClustalW2 is a multiple sequence alignment tool for the alignment of DNA or protein sequences. |
cmake | 2.8.10.2 | cmake/2.8 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.10.3 | cmake/3.10 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.11.3 | cmake/3.11 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.14.5 | cmake/3.14 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.17.0 | cmake/3.17 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.20.5 | cmake/3.20 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.28.3 | cmake/3.28 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.5.0 | cmake/3.5 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cmake | 3.7.1 | cmake/3.7 | None | application | system | CMake is an extensible, open-source system that manages the build process |
cnvcaller | 0.0.2024.01.18 | cnvcaller/2024.01.18 | None | application | computational biology | CNVcaller is designed to detect copy number variation using sequencing data from populations. |
cnvkit | 0.9.10 | cnvkit/0.9 | None | application | bioinformatics | Copy number variant detection from high-throughput sequencing |
cobra | 0.17.1 | cobra/py36/0.17 | None | application | Biology | COBRApy is a package for constraints-based modeling of metabolic networks. |
cobra | 0.17.1 | cobra/py37/0.17 | None | application | Biology | COBRApy is a package for constraints-based modeling of metabolic networks. |
cobra | 0.26.3 | cobra/py38/0.26 | None | application | Biology | COBRApy is a package for constraints-based modeling of metabolic networks. |
cobra | 0.26.3 | cobra/py39/0.26 | None | application | Biology | COBRApy is a package for constraints-based modeling of metabolic networks. |
cobra | 0.26.3 | cobra/py310/0.26 | None | application | Biology | COBRApy is a package for constraints-based modeling of metabolic networks. |
code-server | 4.17.1 | code-server/4.17 | None | application | Development | VS Code in the browser. |
code-server | 4.89.1 | code-server/4.89 | None | application | Development | VS Code in the browser. |
codonw | 1.4.4 | codonw/1.4 | None | application | computational biology | CodonW is a programme designed to simplify the Multivariate analysis (correspondence analysis) of codon and amino acid usage. |
cogent | 3.1 | cogent/3.1 | None | application | computational biology | Cogent is a tool for reconstructing the coding genome using high-quality full-length transcriptome sequences. |
coin-or | 1.8 | coin-or/1.8 | compiler/gcc/9 | library | Open-source mixed integer linear programming solver | |
colony2 | 20230425 | colony2/20230425 | compiler/intel/18 compiler/gcc/9 | application | computational biology | |
compass-cplex | 0.2022.04.02 | compass-cplex/2022.04.02 | None | application | bioinformatics | In-Silico Modeling of Metabolic Heterogeneity using Single-Cell Transcriptomes. |
compiler/clang | 13 | compiler/clang/13 | None | application | compiler | |
compiler/clang | 17 | compiler/clang/17 | None | application | compiler | |
compiler/clang | 18 | compiler/clang/18 | None | application | compiler | |
compiler/gcc | 10 | compiler/gcc/10 | None | application | compiler | |
compiler/gcc | 11 | compiler/gcc/11 | None | application | compiler | |
compiler/gcc | 12 | compiler/gcc/12 | None | application | compiler | |
compiler/gcc | 13.2 | compiler/gcc/13 | None | application | compiler | |
compiler/gcc | 14.2 | compiler/gcc/14 | None | application | compiler | |
compiler/gcc | 9 | compiler/gcc/9 | None | application | compiler | |
compiler/intel | 18 | compiler/intel/18 | None | application | compiler | |
compiler/intel | 19 | compiler/intel/19 | None | application | compiler | |
compiler/intel | 20 | compiler/intel/20 | None | application | compiler | |
compiler/intel | 2021.5 | compiler/intel/2021 | None | application | compiler | |
compiler/intel | 2024.2 | compiler/intel/2024 | None | application | compiler | |
compiler/nvhpc | 21.9 | compiler/nvhpc/21.9 | None | application | compiler | NVIDIA HPC SDK for Linux. |
compiler/nvhpc | 24.5 | compiler/nvhpc/24.5 | None | application | compiler | NVIDIA HPC SDK for Linux. |
compiler/pgi | 18 | compiler/pgi/18 | None | application | compiler | |
compiler/pgi | 19 | compiler/pgi/19 | None | application | compiler | |
compiler/pgi | 20 | compiler/pgi/20 | None | application | compiler | |
compleasm | 0.2.6 | compleasm/0.2 | None | application | bioinformatics | Compleasm: a faster and more accurate reimplementation of BUSCO |
comsol | 5.4 | comsol/5.4 | None | application | simulation | COMSOL Multiphysics |
comsol | 5.5 | comsol/5.5 | None | application | simulation | COMSOL Multiphysics |
comsol | 5.6 | comsol/5.6 | None | application | simulation | COMSOL Multiphysics |
comsol | 6.0 | comsol/6.0 | None | application | simulation | COMSOL Multiphysics |
concoct | 1.1.0 | concoct/1.1 | None | application | Genomics | Clustering cONtigs with COverage and ComposiTion |
conn | 18b | conn/18b | None | application | matlab toolbox | CONN is a Matlab-based cross-platform software for the computation, display, and analysis of functional connectivity in fMRI (fcMRI). |
connectome-workbench | 1.3.2 | connectome-workbench/1.3 | None | application | neuroimaging | Connectome Workbench is an open source, freely available visualization and discovery tool used to map neuroimaging data, especially data generated by the Human Connectome Project |
consurf | 1.0.0 | consurf/1.0 | None | application | Biology | Stand Alone version of ConSurf |
conterminator | 1.c74b5 | conterminator/1.c74b5 | None | application | computational biology | Efficient method for detecting incorrectly labeled sequences across kingdoms |
convert3d | 1.3.0 | convert3d/1.3 | None | application | utility | ITK-based image manipulation tool |
coreutils | 8.31 | coreutils/8.31 | None | application | shell tool | The GNU Core Utilities are the basic file, shell and text manipulation utilities of the GNU operating system. |
corretto-jdk | 11 | corretto-jdk/11 | None | application | system | Amazon Corretto (Java). |
corretto-jdk | 17 | corretto-jdk/17 | None | application | system | Amazon Corretto (Java). |
corretto-jdk | 21 | corretto-jdk/21 | None | application | system | Amazon Corretto (Java). |
corretto-jdk | 22 | corretto-jdk/22 | None | application | system | Amazon Corretto (Java). |
corretto-jdk | 8 | corretto-jdk/8 | None | application | system | Amazon Corretto (Java). |
cosmomvpa | d43b0e7 | cosmomvpa/d43b0e7 | None | application | matlab toolbox | A multi-modal, multi-variate pattern analysis (MVPA) toolbox in Matlab and GNU Octave for cognitive neuroscientists. |
coverm | 0.6.1 | coverm/0.6 | None | application | computational biology | CoverM aims to be a configurable, easy to use and fast DNA read coverage and relative abundance calculator focused on metagenomics applications |
cp2k | 2023.1 | cp2k/2023.1 | compiler/intel/20:openmpi/4.1 compiler/gcc/10:openmpi/4.1 | application | quantum chemistry | Quantum chemistry and solid state physics software package |
cp2k | 2024.3 | cp2k/2024.3 | compiler/intel/20:openmpi/4.1 | application | quantum chemistry | Quantum chemistry and solid state physics software package |
cp2k | 8.2.0 | cp2k/8.2 | compiler/gcc/10:openmpi/4.1 | application | quantum chemistry | Quantum chemistry and solid state physics software package |
cp2k | 9.1 | cp2k/9.1 | compiler/intel/20:openmpi/4.1 | application | quantum chemistry | Quantum chemistry and solid state physics software package |
cp2k | 9.1.0 | cp2k/9.1 | compiler/gcc/10:openmpi/4.1 | application | quantum chemistry | Quantum chemistry and solid state physics software package |
crest | 1.0 | crest/1.0 | None | application | computational biology | |
crossmap | 0.7.0 | crossmap/0.7 | None | application | bioinformatics | CrossMap is a program for convenient conversion of genome coordinates and genome annotation files between assemblies. |
csaw | 1.4 | csaw/1.4 | None | application | computational biology | Detection of differentially bound regions in ChIP-seq data with sliding windows, with methods for normalization and proper FDR control. |
cuda | 10.0 | cuda/10.0 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 10.2 | cuda/10.2 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 11.0 | cuda/11.0 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 11.2 | cuda/11.2 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 11.4 | cuda/11.4 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 11.6 | cuda/11.6 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 11.8 | cuda/11.8 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 12.2 | cuda/12.2 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 6.0 | cuda/6.0 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 6.5 | cuda/6.5 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 7.5 | cuda/7.5 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 8.0 | cuda/8.0 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 9.0 | cuda/9.0 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 9.1 | cuda/9.1 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cuda | 9.2 | cuda/9.2 | None | application | compiler | NVIDIA CUDA Toolkit for Linux. |
cudnn | v5 | cudnn/v5 | None | application | compiler | NVIDIA cuDNN Toolkit for Linux. |
cufflinks | 2.1 | cufflinks/2.1 | None | application | computational biology | Transcriptome assembly and differential expression analysis for RNA-Seq. |
cufflinks | 2.2.1 | cufflinks/2.2 | None | application | computational biology | Transcriptome assembly and differential expression analysis for RNA-Seq. |
curl | 7.50 | curl/7.50 | None | application | network | |
curl | 7.76 | curl/7.76 | compiler/gcc/11 compiler/intel/19 compiler/gcc/10 compiler/intel/20 compiler/gcc/9 compiler/intel/2021 | application | network | |
cutadapt | 1.13 | cutadapt/1.13 | None | application | NGS data | Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads. |
cutadapt | 1.4 | cutadapt/1.4 | None | application | NGS data | Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads. |
cutadapt | 2.8 | cutadapt/2.8 | None | application | NGS data | Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads. |
cutadapt | 2.9 | cutadapt/2.9 | None | application | NGS data | Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads. |
cutruntools | 2020.07.10 | cutruntools/2020.07.10 | None | application | computational biology | CUT&RUNTools is a flexible pipeline for CUT&RUN processing and footprint analysis. |
cytoscape | 3.10.1 | cytoscape/3.10 | None | unknown | unknown | Cytoscape is an open source software platform for visualizing complex networks and integrating these with any type of attribute data. |
cytoscape | 3.6 | cytoscape/3.6 | None | unknown | unknown | Cytoscape is an open source software platform for visualizing complex networks and integrating these with any type of attribute data. |
das_tool | 1.1.2 | das_tool/1.1 | None | application | Genomics | Recovery of genomes from metagenomes via a dereplication,aggregation and scoring strategy. |
dastk | 1.0.0 | dastk/1.0 | None | application | Bioinformatics | Differential ATAC-seq toolkit |
dcm2niix | 1.0.20230411 | dcm2niix/1.0 | None | application | neuroimaging | dcm2niix is a designed to convert neuroimaging data from the DICOM format to the NIfTI format. |
deap | 1.0 | deap/1.0 | None | application | computer science | DEAP is a novel evolutionary computation framework for rapid prototyping and testing of ideas. |
dedalus | 2.1905 | dedalus/py37/2.1905 | None | application | partial differential equation | A flexible framework for solving differential equations using spectral methods. |
dedalus | 2.2006 | dedalus/py37/2.2006 | None | application | partial differential equation | A flexible framework for solving differential equations using spectral methods. |
dedalus | 2.2207.3 | dedalus/2.2207 | compiler/gcc/11:openmpi/4.1 | application | partial differential equation | A flexible framework for solving differential equations using spectral methods. |
dedup | 0.12.8 | dedup/0.12 | None | application | DNA sequencing | DeDup is a tool for read deduplication in paired-end read merging |
deepmd-kit | 2.0.3 | deepmd-kit/2.0 | None | application | molecular dynamics | Deep learning package for many-body potential energy representation and molecular dynamics. |
deepmd-kit | 2.2.5 | deepmd-kit/py39/2.2 | None | application | molecular dynamics | Deep learning package for many-body potential energy representation and molecular dynamics. |
deepmd-kit | 2.2.5 | deepmd-kit/py310/2.2 | None | application | molecular dynamics | Deep learning package for many-body potential energy representation and molecular dynamics. |
deepmd-kit-gpu | 2.0.3 | deepmd-kit-gpu/2.0 | None | application | molecular dynamics | Deep learning package for many-body potential energy representation and molecular dynamics. |
deepmd-kit-gpu | 2.2.5 | deepmd-kit-gpu/py39/2.2 | None | application | molecular dynamics | Deep learning package for many-body potential energy representation and molecular dynamics. |
deepmd-kit-gpu | 2.2.5 | deepmd-kit-gpu/py310/2.2 | None | application | molecular dynamics | Deep learning package for many-body potential energy representation and molecular dynamics. |
deeptools | 2.5.4 | deeptools/2.5 | None | application | computational biology | |
deeptools | 3.0.2 | deeptools/3.0 | None | application | computational biology | |
deeptools | 3.5.1 | deeptools/3.5 | None | application | computational biology | |
deepvirfinder | 2020.11.21 | deepvirfinder/2020.11.21 | None | application | metagenomics | Identifying viruses from metagenomic data by deep learning. |
defiant | 2019.03.02 | defiant/2019.03.02 | None | application | computational biology | Differential methylation, Easy, Fast, Identification and ANnoTation. |
delly | 0.8.3 | delly/0.8 | None | application | Biology | Structural variant discovery by integrated paired-end and split-read analysis |
delly | 0.9.1 | delly/0.9 | None | application | Biology | Structural variant discovery by integrated paired-end and split-read analysis |
delly-omp | 0.8.3 | delly-omp/0.8 | None | application | Biology | Structural variant discovery by integrated paired-end and split-read analysis. |
demultiplex | 1.2.2 | demultiplex/1.2 | None | application | Genomics | Demultiplex any number of FASTA or a FASTQ files based on a list of barcodes |
desman | 2.1 | desman/2.1 | None | application | computational biology | De novo Extraction of Strains from MetAgeNomes |
detectron | 2018.09.11 | detectron/py27/2018.09.11 | None | application | object detection | FAIR's research platform for object detection research, implementing popular algorithms like Mask R-CNN and RetinaNet. |
detectron2 | 0.2.1 | detectron2/py37/0.2 | None | application | object detection | Detectron2 is FAIR's next-generation platform for object detection and segmentation. |
dftd4 | 3.3.0 | dftd4/3.3 | compiler/intel/19 compiler/gcc/10 compiler/gcc/9 compiler/intel/20 | application | Physics | |
diamond | 0.9.25 | diamond/0.9 | None | application | Computational Biology | Accelerated BLAST compatible local sequence aligner |
diamond | 2.0.9 | diamond/2.0 | None | application | Computational Biology | Accelerated BLAST compatible local sequence aligner |
diamond | 2.1.9 | diamond/2.1 | None | application | Computational Biology | Accelerated BLAST compatible local sequence aligner |
diffsplice | 0.1.11 | diffsplice/0.1 | None | application | computational biology | DiffSplice: the Genome-Wide Detection of Differential Splicing Events with RNA-seq |
dmtcp | 2.0 | dmtcp/2.0 | None | application | Utility | |
dmtcp | 2.3 | dmtcp/2.3 | None | application | Utility | |
dmtcp | 2.4 | dmtcp/2.4 | None | application | Utility | |
dmtcp | 2.5 | dmtcp/2.5 | None | application | Utility | |
dmtcp | 2.6 | dmtcp/2.6 | compiler/gcc/10 None compiler/intel/19 compiler/gcc/9 compiler/intel/20 | application | Utility | |
dorado | 0.4.2 | dorado/0.4 | None | application | bioinformatics | Dorado is a high-performance, easy-to-use, open source basecaller for Oxford Nanopore reads. |
dorado | 0.6.0 | dorado/0.6 | None | application | bioinformatics | Dorado is a high-performance, easy-to-use, open source basecaller for Oxford Nanopore reads. |
dorado | 0.7.2 | dorado/0.7 | None | application | bioinformatics | Dorado is a high-performance, easy-to-use, open source basecaller for Oxford Nanopore reads. |
dorado-gpu | 0.4.2 | dorado-gpu/0.4 | None | application | bioinformatics | Dorado is a high-performance, easy-to-use, open source basecaller for Oxford Nanopore reads. |
dorado-gpu | 0.6.0 | dorado-gpu/0.6 | None | application | bioinformatics | Dorado is a high-performance, easy-to-use, open source basecaller for Oxford Nanopore reads. |
dorado-gpu | 0.7.2 | dorado-gpu/0.7 | None | application | bioinformatics | Dorado is a high-performance, easy-to-use, open source basecaller for Oxford Nanopore reads. |
dram | 1.0.6 | dram/1.0 | None | application | genomics | Distilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes |
dram | 1.2.0 | dram/1.2 | None | application | genomics | Distilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes |
dram | 1.5.0 | dram/1.5 | None | application | genomics | Distilled and Refined Annotation of Metabolism: A tool for the annotation and curation of function for microbial and viral genomes |
drep | 2.3.2 | drep/2.3 | None | application | Biology | De-replication of microbial genomes assembled from multiple samples |
dsk | 2.3.3 | dsk/2.3 | None | application | computational biology | DSK is a k-mer counter for reads or genomes. |
dssp | 4.4.7 | dssp/4.4 | None | application | computational biology | Application to assign secondary structure to proteins. |
dtiprep | 1.2 | dtiprep/1.2 | None | application | unknown | DTIPrep is a neuroimaging tool that performs a Study-specific Protocol based automatic pipeline for DWI/DTI quality control and preparation. |
ea-utils | 1.01 | ea-utils/1.0 | None | application | computational biology | EA Utils is a collection of command line tools for processing NextGen sequencing data. Included are fastq-stats and sam-stats which are lightweight tools that display a variety of statistics on fastq and sam files. |
eccodes | 2.24.2 | eccodes/2.24 | compiler/intel/20 compiler/gcc/10 compiler/pgi/20 compiler/intel/19 compiler/gcc/9 | application | package | |
effector-p | 2.0 | effector-p/2.0 | None | application | Biology | EffectorP is a machine learning method for fungal effector prediction in secretomes. |
eggnog-mapper | 2.1.3 | eggnog-mapper/2.1 | None | application | Biology | Fast genome-wide functional annotation through orthology assignment. |
eigen | 3.3.3 | eigen/3.3 | None | application | C++ | C++ template library for linear algebra |
eigen | 3.4.0 | eigen/3.4 | None | application | C++ | C++ template library for linear algebra |
eigensoft | 8.0.0 | eigensoft/8.0 | None | application | genomics | The EIGENSOFT package implements methods for analzing population structure and performing stratification correction |
elk | 8.7.10 | elk/8.7 | compiler/intel/20:openmpi/4.0 | library | runtime support | |
elk | 9.5.1 | elk/9.5 | compiler/intel/20:openmpi/4.0 | library | runtime support | |
emacs | 26.2 | emacs/26.2 | None | application | Utility | GNU Emacs is an extensible, customizable text editor. |
emacs | 27.2 | emacs/27.2 | None | application | Utility | GNU Emacs is an extensible, customizable text editor. |
emacs | 28.2 | emacs/28.2 | None | application | Utility | GNU Emacs is an extensible, customizable text editor. |
emacs | 29.3 | emacs/29.3 | None | application | Utility | GNU Emacs is an extensible, customizable text editor. |
eman2 | 2022.11.06 | eman2/2022.11.06 | compiler/gcc/10:openmpi/4.1 compiler/gcc/9:openmpi/4.1 | application | image processing | A scientific image processing software suite with a focus on CryoEM and CryoET. |
emboss | 6.5.7 | emboss/6.5 | None | application | computational biology | EMBOSS is a free Open Source software analysis package specially developed for the needs of the molecular biology (e.g. EMBnet) user community. |
emboss | 6.6.0 | emboss/6.6 | None | application | computational biology | EMBOSS is a free Open Source software analysis package specially developed for the needs of the molecular biology (e.g. EMBnet) user community. |
emirge | 0.61.1 | emirge/0.61 | None | application | Biology | EMIRGE reconstructs full length ribosomal genes from short read sequencing data. |
ensembl-vep | 104.3 | ensembl-vep/104.3 | None | application | Biology | The VEP determines the effect of your variants (SNPs, insertions, deletions, CNVs or structural variants) on genes, transcripts, and protein sequence, as well as regulatory regions. |
ensembl-vep | 96.0 | ensembl-vep/96.0 | None | application | Biology | The VEP determines the effect of your variants (SNPs, insertions, deletions, CNVs or structural variants) on genes, transcripts, and protein sequence, as well as regulatory regions. |
ensembl-vep | 99.2 | ensembl-vep/99.2 | None | application | Biology | The VEP determines the effect of your variants (SNPs, insertions, deletions, CNVs or structural variants) on genes, transcripts, and protein sequence, as well as regulatory regions. |
entrez-direct | 10.0 | entrez-direct/10.0 | None | application | Entrez | Entrez Direct (EDirect) is an advanced method for accessing the NCBI's set of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNIX terminal window. |
entrez-direct | 11.0 | entrez-direct/11.0 | None | application | Entrez | Entrez Direct (EDirect) is an advanced method for accessing the NCBI's set of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNIX terminal window. |
entrez-direct | 13.3 | entrez-direct/13.3 | None | application | Entrez | Entrez Direct (EDirect) is an advanced method for accessing the NCBI's set of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNIX terminal window. |
entrez-direct | 16.2 | entrez-direct/16.2 | None | application | Entrez | Entrez Direct (EDirect) is an advanced method for accessing the NCBI's set of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNIX terminal window. |
epic2 | 0.0.50 | epic2/0.0.50 | None | application | Biology | Ultraperformant Chip-Seq broad domain finder based on SICER. |
epivia | 1.1.2 | epivia/1.1 | None | application | Epigenomics | Virial Integration Analysis with epigenetic data |
epoch | 4.17.16 | epoch/4.17 | compiler/intel/20:openmpi/4.0 | application | Applications | |
epoch | 4.17.16 | epoch/4.19 | compiler/intel/20:openmpi/4.0 | application | Applications | |
eqtlbma | 1.3 | eqtlbma/1.3 | None | application | biology | Package to detect eQTLs jointly in multiple subgroups (e.g. tissues) via Bayesian Model Averaging. |
erne | 2.1.1 | erne/2.1 | None | application | computational biology | ERNE is a short string alignment package whose goal is to provide an all-inclusive set of tools to handle short (NGS-like) reads. |
esmf | 8.2.0 | esmf/8.2 | compiler/intel/19:openmpi/4.0 | application | Utility | |
espresso | 6.8 | espresso/6.8 | compiler/intel/20:openmpi/4.0 compiler/intel/20:openmpi/4.1 | library | runtime support | |
espresso | 7.0 | espresso/7.0 | compiler/intel/20:openmpi/4.1 | library | runtime support | |
espresso | 7.1 | espresso/7.1 | compiler/intel/20:openmpi/4.1 compiler/intel/20:openmpi/4.0 | library | runtime support | |
espresso | 7.3 | espresso/7.3 | compiler/intel/20:openmpi/4.1 compiler/intel/20:openmpi/4.0 | library | runtime support | |
espresso-gpu | 7.1 | espresso-gpu/7.1 | compiler/nvhpc/21.9:openmpi/3.1 | library | runtime support | |
espresso-gpu | 7.3 | espresso-gpu/7.3 | compiler/nvhpc/21.9:openmpi/3.1 | library | runtime support | |
espresso-plumed | 6.2 | espresso-plumed/6.2 | compiler/intel/20:openmpi/4.1 | library | runtime support | |
ete3 | 3.1.1 | ete3/3.1 | None | application | NCBI | Python package for building, comparing, annotating, manipulating and visualising trees. It provides a comprehensive API and a collection of command line tools, including utilities to work with the NCBI taxonomy tree. |
evidencemodeler | 1.1.1 | evidencemodeler/1.1 | None | application | computational biology | EVidence Modeler. |
exomiser | 7.2 | exomiser/7.2 | None | application | computational biology | The Exomiser is a Java program that finds potential disease-causing variants from whole-exome or whole-genome sequencing data. |
exonerate | 2.2.0 | exonerate/2.2 | None | application | computational biology | Exonerate - A generic tool for pairwise sequence comparison / alignment |
exonerate | 2.4.0 | exonerate/2.4 | None | application | computational biology | Exonerate - A generic tool for pairwise sequence comparison / alignment |
expansionhunterdenovo | 0.9.0 | expansionhunterdenovo/0.9 | None | application | computational biology | ExpansionHunter Denovo (EHdn) is a suite of tools for detecting novel expansions of short tandem repeats (STRs). |
expat | 2.2.9 | expat/2.2 | compiler/pgi/20 compiler/intel/20 compiler/gcc/9 compiler/intel/19 compiler/gcc/10 | library | runtime support | |
export2graphlan | 0.20 | export2graphlan/0.20 | None | application | bioinformatics | export2graphlan is a conversion software tool for producing both annotation and tree file for GraPhlAn. |
express | 1.5 | express/1.5 | None | application | life sciences | express - Streaming quantification for high-throughput sequencing |
fair-esm | 2.0.0 | fair-esm/py39/2.0 | None | application | evolutionary modeling | Evolutionary Scale Modeling (esm): Pretrained language models for proteins. From Facebook AI Research. |
fair-esm | 2.0.0 | fair-esm/py310/2.0 | None | application | evolutionary modeling | Evolutionary Scale Modeling (esm): Pretrained language models for proteins. From Facebook AI Research. |
fair-esm-gpu | 2.0.0 | fair-esm-gpu/py39/2.0 | None | application | evolutionary modeling | Evolutionary Scale Modeling (esm): Pretrained language models for proteins. From Facebook AI Research. |
fair-esm-gpu | 2.0.0 | fair-esm-gpu/py310/2.0 | None | application | evolutionary modeling | Evolutionary Scale Modeling (esm): Pretrained language models for proteins. From Facebook AI Research. |
fargene | 0.1 | fargene/0.1 | None | application | bioinformatics | Fragmented Antibiotic Resistance Gene iENntifiEr takes either fragmented metagenomic data or longer sequences as input and predicts and delivers full-length antiobiotic resistance genes as output |
fastani | 1.32 | fastani/1.32 | None | application | Biology | FastANI is developed for fast alignment-free computation of whole-genome Average Nucleotide Identity (ANI). |
fastcluster | 1.2.6 | fastcluster/py39/1.2 | None | application | machine learning | Fast hierarchical clustering routines for R and Python. |
fastcluster | 1.2.6 | fastcluster/py310/1.2 | None | application | machine learning | Fast hierarchical clustering routines for R and Python. |
fastp | 0.23.2 | fastp/0.23 | None | application | bioinformatics | A ultra-fast FASTQ preprocessor with full features (QC/adapters/trimming/filtering/splitting...) |
fastq-screen | 0.15.3 | fastq-screen/0.15 | None | application | computational biology | FastQ Screen allows you to screen a library of sequences in FastQ format against a set of sequence databases so you can see if the composition of the library matches with what you expect |
fastq_utils | 0.25.2 | fastq_utils/0.25 | None | application | Genomics | Validation and manipulation of FASTQ files, scRNA-seq barcode pre-processing and UMI quantification. |
fastqc | 0.10.1 | fastqc/0.10 | None | application | computational biology | fastqc - A Quality Control application for FastQ files |
fastqc | 0.11.7 | fastqc/0.11 | None | application | computational biology | fastqc - A Quality Control application for FastQ files |
fastqc | 0.12.1 | fastqc/0.12 | None | application | computational biology | fastqc - A Quality Control application for FastQ files |
fastspar | 0.0.10 | fastspar/0.0.10 | None | application | computational biology | Rapid and scalable correlation estimation for compositional data |
faststructure | 1.0 | faststructure/1.0 | None | application | computational biology | A variational framework for inferring population structure from SNP genotype data. |
fasttree | 2.1.11 | fasttree/2.1 | None | application | computational biology | FastTree infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences. |
fastx_toolkit | 0.0.14 | fastx_toolkit/0.0.14 | None | application | computational biology | FASTX Toolkit is a collection of command line tools for Short-Reads FASTA/FASTQ files preprocessing. |
fegenie | 1.0 | fegenie/1.0 | None | application | genomics | HMM-based identification and categorization of iron genes and iron gene operons in genomes and metagenomes. |
feh | 3.3 | feh/3.3 | None | application | Utility | feh is an X11 image viewer aimed mostly at console users. |
feh | 3.9.1 | feh/3.9 | None | application | Utility | feh is an X11 image viewer aimed mostly at console users. |
fenics | 2018.1.0 | fenics/2018.1 | None | application | partial differential equations | FEniCS is a collection of free software for automated, efficient solution of differential equations |
ffmpeg | 4.3.1 | ffmpeg/4.3 | None | application | Utility | Cross-platform solution to record, convert and stream audio and video. |
ffmpeg | 4.4.1 | ffmpeg/4.4 | None | application | Utility | Cross-platform solution to record, convert and stream audio and video. |
fftw3 | 3.3 | fftw3/3.3 | compiler/gcc/10 compiler/gcc/9:openmpi/4.0 compiler/intel/19:openmpi/4.1 compiler/gcc/11 compiler/intel/20:openmpi/4.0 compiler/intel/18:openmpi/4.0 compiler/gcc/10:openmpi/4.0 compiler/intel/19:openmpi/4.0 compiler/gcc/10:openmpi/4.1 compiler/intel/18:openmpi/4.1 compiler/intel/19 compiler/pgi/20 compiler/gcc/11:openmpi/4.0 compiler/pgi/20:openmpi/4.1 compiler/gcc/9:openmpi/4.1 compiler/intel/18 compiler/intel/20:openmpi/4.1 compiler/intel/20 compiler/gcc/9 None compiler/pgi/20:openmpi/4.0 compiler/gcc/11:openmpi/4.1 | library | runtime support | |
fgbio | 0.8.0 | fgbio/0.8 | None | application | Genomics | A set of tools for working with genomic and high throughput sequencing data, including UMIs |
figtree | 1.4.4 | figtree/1.4 | None | application | Utilities | FigTree is designed as a graphical viewer of phylogenetic trees and as a program for producing publication-ready figures. |
fiji | 20220414 | fiji/20220414 | None | application | Image Processing | Fiji is an image processing package—a 'batteries-included' distribution of ImageJ, bundling a lot of plugins which facilitate scientific image analysis. |
flash | 1.2.11 | flash/1.2 | None | application | bioinformatics | Merge paired sequencing reads into single longer sequences |
flash2 | 2.2.00 | flash2/2.2 | None | application | bioinformatics | Merge paired-end reads from fragments that are shorter than twice the read length |
fleur | 6.2 | fleur/6.2 | compiler/gcc/11:openmpi/4.1 | application | physics | A feature-full, freely available FLAPW (full-potential linearized augmented planewave) code, based on density-functional theory. |
fleur | 7.0 | fleur/7.0 | compiler/gcc/9:openmpi/4.1 | application | physics | A feature-full, freely available FLAPW (full-potential linearized augmented planewave) code, based on density-functional theory. |
flex | 3.7.5 | flex/2.6 | None | application | Utility | General purpose parser generator converting annotated context-free grammar to a deterministic LR/GLR parser. |
flye | 2.8.3 | flye/2.8 | None | application | Bioinformatics | Fast and accurate de novo assembler for single molecule sequencing reads |
flye | 2.9.1 | flye/2.9 | None | application | Bioinformatics | Fast and accurate de novo assembler for single molecule sequencing reads |
foldseek | 8.ef4e960 | foldseek/8.ef4e960 | None | application | computational bioinformatics | Foldseek: fast and accurate protein structure search |
foldseek | 9.427df8a | foldseek/9.427df8a | None | application | computational bioinformatics | Foldseek: fast and accurate protein structure search |
fonduer | 0.8.2 | fonduer/py37/0.8 | None | application | knowledge base | Fonduer is a Python package and framework for building knowledge base construction (KBC) applications from richly formatted data. |
fortrangis | 2.5 | fortrangis/2.5 | compiler/gcc/10 compiler/intel/20 compiler/gcc/9 compiler/intel/19 | library | runtime support | |
fqtrim | 0.9.7 | fqtrim/0.9 | None | application | computational biology | fqtrim: trimming & filtering of NGS reads. |
fragpipe | 20.0 | fragpipe/20.0 | None | application | mass spectrometry | Pipeline for comprehensive analysis of shotgun proteomics data |
freebayes | 1.2.0 | freebayes/1.2 | None | application | Biology | Bayesian haplotype-based polymorphism discovery and genotyping |
freebayes | 1.3.7 | freebayes/1.3 | None | application | Biology | Bayesian haplotype-based polymorphism discovery and genotyping |
freecad | 0.20.1 | freecad/0.20 | None | application | 3D modeling | FreeCAD is a parametric 3D modeler made primarily to design real-life objects of any size. |
freesurfer | 5.3.0 | freesurfer/5.3 | None | application | computational neuroimaging | An open source software suite for processing and analyzing (human) brain MRI images. |
freesurfer | 6.0.1 | freesurfer/6.0 | None | application | computational neuroimaging | An open source software suite for processing and analyzing (human) brain MRI images. |
freesurfer | 7.1.1 | freesurfer/7.1 | None | application | computational neuroimaging | An open source software suite for processing and analyzing (human) brain MRI images. |
freesurfer | 7.2.0 | freesurfer/7.2 | None | application | computational neuroimaging | An open source software suite for processing and analyzing (human) brain MRI images. |
freesurfer | 7.4.1 | freesurfer/7.4 | None | application | computational neuroimaging | An open source software suite for processing and analyzing (human) brain MRI images. |
freetype | 2.10.0 | freetype/2.10 | compiler/intel/20 compiler/pgi/20 | library | runtime support | |
fsl | 6.0.6 | fsl/6.0 | None | application | computational neuroimaging | FMRIB Software Library |
fusioncatcher | 1.33 | fusioncatcher/1.33 | None | application | computational biology | Finder of Somatic Fusion Genes in RNA-seq data. |
gamess | 20210930R2 | gamess/20210930R2 | compiler/intel/2021:intel-mpi/2021 compiler/intel/19:openmpi/4.0 | library | runtime support | |
gamess-omp | 20210930R2 | gamess-omp/20210930R2 | compiler/intel/19:openmpi/4.0 | library | runtime support | |
gap | 4.11.0 | gap/4.11 | None | application | Mathematics | GAP - Groups, Algorithms, Programming, a System for Computational Discrete Algebra |
gapfiller | 2.1.1 | gapfiller/2.1 | None | application | computational biology | GapFiller is a seed-and-extend local assembler to fill the gap within paired reads. |
gat | 1.3.6 | gat/1.3 | None | application | Biology | Genomic Association Tester |
gatk | 3.4-46 | gatk/3.4 | None | application | computational biology | The Genome Analysis Toolkit or GATK is a software package developed at the Broad Institute to analyze high-throughput sequencing data. The toolkit offers a wide variety of tools, with a primary focus on variant discovery and genotyping as well as strong emphasis on data quality assurance. Its robust architecture, powerful processing engine and high-performance computing features make it capable of taking on projects of any size. |
gatk | 3.7 | gatk/3.7 | None | application | computational biology | The Genome Analysis Toolkit or GATK is a software package developed at the Broad Institute to analyze high-throughput sequencing data. The toolkit offers a wide variety of tools, with a primary focus on variant discovery and genotyping as well as strong emphasis on data quality assurance. Its robust architecture, powerful processing engine and high-performance computing features make it capable of taking on projects of any size. |
gatk4 | 4.0.4.0 | gatk4/4.0 | None | application | computational biology | GATK4: This toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. |
gatk4 | 4.1.8.1 | gatk4/4.1 | None | application | computational biology | GATK4: This toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. |
gatk4 | 4.2.4.1 | gatk4/4.2 | None | application | computational biology | GATK4: This toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. |
gatk4 | 4.3.0.0 | gatk4/4.3 | None | application | computational biology | GATK4: This toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. |
gatk4 | 4.4.0.0 | gatk4/4.4 | None | application | computational biology | GATK4: This toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. |
gaussian | 09 RevD | gaussian/09/RevD | None | application | Chemistry | |
gaussian | 09 RevE | gaussian/09/RevE | None | application | Chemistry | |
gaussian | 16 RevA | gaussian/16/RevA | None | application | Chemistry | |
gbmunge | 2018.07.06 | gbmunge/2018.07.06 | None | application | computational biology | Munge GenBank files into FASTA and tab-separated metadata. |
gcprofile | 1.0 | gcprofile/1.0 | None | application | computational biology | GC-Profile is a web-based tool for visualizing and analyzing the variation of GC content in genomic sequences |
gcta | 1.94.1 | gcta/1.94 | None | application | computational biology | GCTA (Genome-wide Complex Trait Analysis) estimates the proportion of phenotypic variance explained by all genome-wide SNPs for complex traits. |
gdal | 3.4 | gdal/3.4 | compiler/gcc/10 compiler/gcc/9 compiler/intel/20 compiler/intel/19 | library | runtime support | |
gdcclient | 1.3.0 | gdcclient/1.3 | None | application | genomics | GDC provides a standard client-based mechanism in support of high performance data downloads and submission. |
gdcclient | 1.4.0 | gdcclient/1.4 | None | application | genomics | GDC provides a standard client-based mechanism in support of high performance data downloads and submission. |
gdcclient | 1.6.1 | gdcclient/1.6 | None | application | genomics | GDC provides a standard client-based mechanism in support of high performance data downloads and submission. |
gem | 2.7 | gem/2.7 | None | application | computational biology | GEM: High resolution peak calling and motif discovery for ChIP-seq and ChIP-exo data. |
gemma | 0.98.1 | gemma/0.98 | None | application | computational biology | Linear mixed models (LMMs) for genome-wide association (GWA) |
gemoma | 1.9 | gemoma/1.9 | None | application | Genome Analysis | Gene Model Mapper (GeMoMa) is a homology-based gene prediction program. |
genemark-es | 2.3f | genemark-es/2.3f | None | application | computational biology | GeneMark-ES. |
genemarks | 2.5p | genemarks/2.5p | None | application | computational biology | GeneMarkS: a self-training method for prediction of gene starts in microbial genomes. Implications for finding sequence motifs in regulatory regions |
genemarks | 4.3 | genemarks/4.3 | None | application | computational biology | GeneMarkS: a self-training method for prediction of gene starts in microbial genomes. Implications for finding sequence motifs in regulatory regions |
genodiver | 2018.11.12 | genodiver/2018.11.12 | None | application | biology | Geno-Diver is a complex animal genetic simulation tool that is able to simulate quantitative and/or fitness characters. |
genometester4 | 4.0 | genometester4/4.0 | None | application | Bioinformatics | A toolkit for performing set operations - union, intersection and complement - on k-mer lists. |
genometools/py27 | 1.5.10 | genometools/py27/1.5 | None | application | Bioinformatics | GenomeTools genome analysis system. |
genometools/py35 | 1.5.10 | genometools/py35/1.5 | None | application | Bioinformatics | GenomeTools genome analysis system. |
genometools/py36 | 1.5.10 | genometools/py36/1.5 | None | application | Bioinformatics | GenomeTools genome analysis system. |
genozip | 14.0.21 | genozip/14.0 | None | application | computational biology | Compressor for genomic files (FASTQ, BAM, VCF, FASTA and more), up to 5x better than gzip and faster too |
gensim | 3.8.0 | gensim/py27/3.8 | None | application | Machine learning | Topic Modelling for Humans |
gensim | 3.8.0 | gensim/py36/3.8 | None | application | Machine learning | Topic Modelling for Humans |
gensim | 3.8.0 | gensim/py37/3.8 | None | application | Machine learning | Topic Modelling for Humans |
geodata | 1.0 | geodata/1.0 | None | application | geo models | Static data resources for geo data. |
geoparse | 1.0.5 | geoparse/1.0 | None | application | Bioinformatics | Python library to access Gene Expression Omnibus Database (GEO) |
geos | 3.8 | geos/3.8 | compiler/gcc/10 compiler/pgi/20 compiler/gcc/9 compiler/intel/20 compiler/intel/19 | library | runtime support | |
getorganelle | 1.7.7.1 | getorganelle/1.7 | None | application | bioinformatics | Get organelle genomes from genome skimming data |
gffcompare | 0.10.6 | gffcompare/0.10 | None | application | Annotation | GffCompare by Geo Pertea |
gffread | 0.12.7 | gffread/0.12 | None | application | bioinformatics | GFF/GTF utility providing format conversions, region filtering, FASTA sequence extraction and more. |
gflags | 2.1 | gflags/2.1 | None | library | unknown | Online documentation available at: https://gflags.github.io/gflags/ |
ghostscript | 9.20 | ghostscript/9.20 | None | library | runtime support | An interpreter for the PostScript language and for PDF. |
ghostscript | 9.22 | ghostscript/9.22 | None | library | runtime support | An interpreter for the PostScript language and for PDF. |
gistic2 | 2.0.23 | gistic2/2.0 | None | application | Biology | GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers. |
git | 2.17.0 | git/2.17 | None | library | tools | distributed version control system |
git | 2.22.0 | git/2.22 | None | library | tools | distributed version control system |
git | 2.29.2 | git/2.29 | None | library | tools | distributed version control system |
git | 2.30.9 | git/2.30 | None | library | tools | distributed version control system |
git | 2.35.8 | git/2.35 | None | library | tools | distributed version control system |
git | 2.39.3 | git/2.39 | None | library | tools | distributed version control system |
git | 2.40.1 | git/2.40 | None | library | tools | distributed version control system |
git | 2.7.4 | git/2.7 | None | library | tools | distributed version control system |
globalarrays | 5.8.2 | globalarrays/5.8 | compiler/gcc/11:openmpi/4.1 compiler/gcc/9:openmpi/4.1 compiler/intel/20:openmpi/4.1 compiler/intel/19:openmpi/4.1 compiler/intel/2021:openmpi/4.1 compiler/gcc/10:openmpi/4.1 | library | runtime support | |
globus-cli | 1.10.1 | globus-cli/1.10 | None | application | tool | Globus CLI |
globus-cli | 1.13.0 | globus-cli/1.13 | None | application | tool | Globus CLI |
globus-cli | 1.2.0 | globus-cli/1.2 | None | application | tool | Globus CLI |
globus-cli | 2.0.0 | globus-cli/2.0 | None | application | tool | Globus CLI |
globus-cli | 3.18.0 | globus-cli/3.0 | None | application | tool | Globus CLI |
glog | 0.3.3 | glog/0.3 | None | application | Utility | |
glpk | 4.61 | glpk/4.61 | None | application | mathematics | The GLPK (GNU Linear Programming Kit) package is intended for solving large-scale linear programming (LP), mixed integer programming (MIP), and other related problems. It is a set of routines written in ANSI C and organized in the form of a callable library. |
gmap | 2015.12.31 | gmap/2015.12.31 | None | application | computational biology | GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences, and GSNAP: Genomic Short-read Nucleotide Alignment Program. |
gmap | 2017.05.08 | gmap/2017.05.08 | None | application | computational biology | GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences, and GSNAP: Genomic Short-read Nucleotide Alignment Program. |
gmap | 2018.03.25 | gmap/2018.03.25 | None | application | computational biology | GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences, and GSNAP: Genomic Short-read Nucleotide Alignment Program. |
gmap | 2020.04.08 | gmap/2020.04.08 | None | application | computational biology | GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences, and GSNAP: Genomic Short-read Nucleotide Alignment Program. |
gmap | 2021.08.25 | gmap/2021.08.25 | None | application | computational biology | GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences, and GSNAP: Genomic Short-read Nucleotide Alignment Program. |
gmap | 2023.10.10 | gmap/2023.10.10 | None | application | computational biology | GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences, and GSNAP: Genomic Short-read Nucleotide Alignment Program. |
gmcloser | 1.6.2 | gmcloser/1.6 | None | application | computational biology | GMcloser fills and closes the gaps present in scaffold assemblies, especially those generated by the de novo assembly of whole genomes with next-generation sequencing (NGS) reads. |
gmp | 6.2.1 | gmp/6.2 | compiler/pgi/20 compiler/gcc/9 compiler/intel/20 compiler/intel/19 compiler/gcc/10 | library | runtime support | GNU MP is a library for arbitrary precision arithmetic, operating on signed integers, rational numbers, and floating point numbers. |
gmx_mmpbsa | 1.6.3 | gmx_mmpbsa/1.6 | compiler/gcc/11:openmpi/4.1 | application | computational chemistry | gmx_MMPBSA is a new tool based on AMBER's MMPBSA.py aiming to perform end-state free energy calculations with GROMACS files. |
gnu-parallel | 20180522 | gnu-parallel/20180522 | None | application | Shell tool | GNU parallel is a shell tool for executing jobs in parallel using one or more computers. |
gnu-parallel | 20220722 | gnu-parallel/20220722 | None | application | Shell tool | GNU parallel is a shell tool for executing jobs in parallel using one or more computers. |
gnuplot | 4.6.0 | gnuplot/4.6 | None | application | unknown | Gnuplot, plotting from command line |
gnuplot | 5.2.3 | gnuplot/5.2 | None | application | unknown | Gnuplot, plotting from command line |
gnuplot | 5.4.1 | gnuplot/5.4 | None | application | unknown | Gnuplot, plotting from command line |
google-cloud-sdk | 350.0.0 | google-cloud-sdk/350 | None | application | Utility | Command-line interface for Google Cloud Platform products and services |
google-cloud-sdk | 440.0.0 | google-cloud-sdk/440 | None | application | Utility | Command-line interface for Google Cloud Platform products and services |
gradle | 3.3 | gradle/3.3 | None | application | Utility | Gradle - an open-source build-automation system |
gradle | 5.6 | gradle/5.6 | None | application | Utility | Gradle - an open-source build-automation system |
gradle | 7.1.0 | gradle/7.1 | None | application | Utility | Gradle - an open-source build-automation system |
gramalign | 3.0 | gramalign/3.0 | None | application | computational biology | GramAlign is a time-efficient progressive Multiple Sequence Alignment (MSA) algorithm. |
gramcluster | 1.3 | gramcluster/1.3 | None | application | computational biology | GramCluster is a fast and accurate progressive clustering algorithm that relies on a grammar-based sequence distance and is particularly useful in clustering large datasets. |
gramdist | 1.0 | gramdist/1.0 | None | application | computational biology | GramDist is a utility for generating dissimilarity matrices using the relative complexity measure, a computationally efficient and alignment free evolutionary distance metric. |
graphlan | 1.0.0 | graphlan/1.0 | None | application | computational biology | GraPhlAn is a software tool for producing high-quality circular representations of taxonomic and phylogenetic trees. It focuses on concise, integrative, informative, and publication-ready representations of phylogenetically- and taxonomically-driven investigation. |
graphlan | 1.1.2 | graphlan/1.1 | None | application | computational biology | GraPhlAn is a software tool for producing high-quality circular representations of taxonomic and phylogenetic trees. It focuses on concise, integrative, informative, and publication-ready representations of phylogenetically- and taxonomically-driven investigation. |
graphviz | 2.38.0 | graphviz/2.38 | None | application | Visualization | Open Source graph visualization software. |
graphviz | 2.40.1 | graphviz/2.40 | None | application | Visualization | Open Source graph visualization software. |
graphviz | 4.0.0 | graphviz/4.0 | None | application | Visualization | Open Source graph visualization software. |
grib-api | 1.21.0 | grib-api/1.21 | compiler/pgi/20 compiler/intel/20 | library | runtime support | |
gromacs | 2022.3 | gromacs/2022.3 | compiler/gcc/10:openmpi/4.1 | application | computational biology | GROMACS is a versatile package to perform molecular dynamics, i.e. simulate the Newtonian equations of motion for systems with hundreds to millions of particles. |
gromacs | 2023 | gromacs/2023 | compiler/gcc/10:openmpi/4.1 | application | computational biology | GROMACS is a versatile package to perform molecular dynamics, i.e. simulate the Newtonian equations of motion for systems with hundreds to millions of particles. |
gromacs | 2024.1 | gromacs/2024.1 | compiler/gcc/11:openmpi/4.1 | application | computational biology | GROMACS is a versatile package to perform molecular dynamics, i.e. simulate the Newtonian equations of motion for systems with hundreds to millions of particles. |
gromacs-gpu | 2021.1 | gromacs-gpu/2021.1 | compiler/gcc/9 | application | computational biology | GROMACS is a versatile package to perform molecular dynamics, i.e. simulate the Newtonian equations of motion for systems with hundreds to millions of particles. |
gromacs-gpu | 2022.3 | gromacs-gpu/2022.3 | compiler/gcc/10 | application | computational biology | GROMACS is a versatile package to perform molecular dynamics, i.e. simulate the Newtonian equations of motion for systems with hundreds to millions of particles. |
gromacs-gpu | 2023 | gromacs-gpu/2023 | compiler/gcc/10 compiler/gcc/10:openmpi/4.1 | application | computational biology | GROMACS is a versatile package to perform molecular dynamics, i.e. simulate the Newtonian equations of motion for systems with hundreds to millions of particles. |
gromacs-gpu | 2024.1 | gromacs-gpu/2024.1 | compiler/gcc/11 compiler/gcc/11:openmpi/4.1 | application | computational biology | GROMACS is a versatile package to perform molecular dynamics, i.e. simulate the Newtonian equations of motion for systems with hundreds to millions of particles. |
groopm | 0.3.4 | groopm/0.3 | None | application | bioinformatics | Metagenomic binning suite |
gstreamer | 1.20.3 | gstreamer/1.20 | None | application | Library for constructing graphs of media-handling components | Library for constructing graphs of media-handling components |
gstreamer | 1.22.5 | gstreamer/1.22 | None | application | Library for constructing graphs of media-handling components | Library for constructing graphs of media-handling components |
gsufsort | 2023.10.20 | gsufsort/2023.10.20 | None | application | bioinformatics | Building suffix arrays, LCP-arrays and BWTs for string collections. |
gsutil | 350.0.0 | gsutil/4.65 | None | application | Utility | Command-line interface for Google Cloud Platform products and services |
gsutil | 440.0.0 | gsutil/5.25 | None | application | Utility | Command-line interface for Google Cloud Platform products and services |
gtdbtk | 0.1.3 | gtdbtk/0.1 | None | application | computational biology | A toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes. |
gtdbtk | 1.3.0 | gtdbtk/1.3 | None | application | computational biology | A toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes. |
gtdbtk | 1.5.0 | gtdbtk/1.5 | None | application | computational biology | A toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes. |
gubbins | 2.3.4 | gubbins/2.3 | None | application | Biology | Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins. |
gubbins | 3.1.6 | gubbins/3.1 | None | application | Biology | Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins. |
guppy | 6.2.1 | guppy/6.2 | None | application | Bioinformatics | Guppy is a data processing toolkit that contains the Oxford Nanopore Technologies’ basecalling algorithms, and several bioinformatic post-processing features. |
guppy | 6.3.4 | guppy/6.3 | None | application | Bioinformatics | Guppy is a data processing toolkit that contains the Oxford Nanopore Technologies’ basecalling algorithms, and several bioinformatic post-processing features. |
guppy | 6.5.7 | guppy/6.5 | None | application | Bioinformatics | Guppy is a data processing toolkit that contains the Oxford Nanopore Technologies’ basecalling algorithms, and several bioinformatic post-processing features. |
guppy-gpu | 6.2.1 | guppy-gpu/6.2 | None | application | Bioinformatics | Guppy is a data processing toolkit that contains the Oxford Nanopore Technologies’ basecalling algorithms, and several bioinformatic post-processing features. |
guppy-gpu | 6.3.4 | guppy-gpu/6.3 | None | application | Bioinformatics | Guppy is a data processing toolkit that contains the Oxford Nanopore Technologies’ basecalling algorithms, and several bioinformatic post-processing features. |
guppy-gpu | 6.5.7 | guppy-gpu/6.5 | None | application | Bioinformatics | Guppy is a data processing toolkit that contains the Oxford Nanopore Technologies’ basecalling algorithms, and several bioinformatic post-processing features. |
gurobi | 10.0.2 | gurobi/py39/10.0 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi | 10.0.2 | gurobi/py310/10.0 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi | 11.0.0 | gurobi/py39/11.0 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi | 11.0.0 | gurobi/py310/11.0 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi | 9.0.3 | gurobi/py36/9.0 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi | 9.0.3 | gurobi/py37/9.0 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi | 9.5.1 | gurobi/py38/9.5 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi | 9.5.1 | gurobi/py39/9.5 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi-python | 8.1.0 | gurobi-python/py27/8.1 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi-python | 8.1.0 | gurobi-python/py35/8.1 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
gurobi-python | 8.1.0 | gurobi-python/py36/8.1 | None | application | Mathematics | The Gurobi Optimizer is the state-of-the-art math programming solver able to handle all major problem types. |
halla | 0.8.17 | halla/0.8 | None | application | computational biology | HAllA: Hierarchically All-against-All Association Testing. |
hapflk | 1.3.0 | hapflk/1.3 | None | application | package | hapflk is a software implementing the hapFLK [1] and FLK [2] tests for the detection of selection signatures based on multiple population genotyping data. |
hapsolo | 2021.10.09 | hapsolo/2021.10.09 | None | application | computational biology | An optimization approach for removing secondary haplotigs during diploid genome assembly and scaffolding. |
haptools | 0.4.0 | haptools/0.4 | None | application | bioinformatics | Ancestry and haplotype aware simulation of genotypes and phenotypes for complex trait analysis |
haskell-platform | 8.2.1 | haskell-platform/8.2.1 | None | application | Utilities | The Haskell Platform is a collection of software packages, tools and libraries that create a common platform for using and developing applications in Haskell.. |
haslr | 0.8a1 | haslr/0.8a1 | None | application | genomics | A fast tool for hybrid genome assembly of long and short reads |
hdf-eos2 | 2.20 | hdf-eos2/2.20 | compiler/pgi/20 compiler/intel/19 compiler/gcc/10 compiler/gcc/9 compiler/intel/20 | library | runtime support | |
hdf4 | 4.2.15 | hdf4/4.2 | compiler/pgi/20 compiler/intel/19 compiler/intel/20 compiler/gcc/10 compiler/gcc/9 | library | runtime support | |
hdf5 | 1.12 | hdf5/1.12 | compiler/gcc/11 compiler/intel/19 compiler/intel/18 compiler/gcc/10 compiler/intel/20 compiler/gcc/9 compiler/pgi/20 | library | runtime support | |
hdf5 | 1.8 | hdf5/1.8 | compiler/intel/18 compiler/gcc/9 None | library | runtime support | |
hiddendomains | 2.3 | hiddendomains/2.3 | None | application | chip-seq | hiddenDomains is a suite of programs used to identify significant enrichment of ChIP-seq reads that span large domains. |
hifiasm | 0.19.8 | hifiasm/0.19 | None | application | computational biology | Haplotype-resolved assembler for accurate Hifi reads |
hisat2 | 2.0.5 | hisat2/2.0 | None | application | computational biology | graph-based alignment of next generation sequencing reads to a population of genomes |
hisat2 | 2.1.0 | hisat2/2.1 | None | application | computational biology | graph-based alignment of next generation sequencing reads to a population of genomes |
hisat2 | 2.2.1 | hisat2/2.2 | None | application | computational biology | graph-based alignment of next generation sequencing reads to a population of genomes |
hmmer | 3.3.1 | hmmer/3.3 | compiler/gcc/9:openmpi/4.0 compiler/gcc/11:openmpi/4.1 | application | computational biology | HMMER biosequence analysis using profile hidden Markov models |
homer | 4.11 | homer/4.11 | None | application | computational biology | Software for motif discovery and next generation sequencing analysis |
hotspot3d | 0.6.0 | hotspot3d/0.6 | None | application | bioinformatics | This 3D proximity tool can be used to identify mutation hotspots from linear protein sequence and correlate the hotspots with known or potentially interacting domains, mutations, or drugs. Mutation-mutation and mutation-drug clusters can also be identified and viewed. |
htseq | 0.11.2 | htseq/py27/0.11 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 0.11.2 | htseq/py36/0.11 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 0.11.2 | htseq/py37/0.11 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 0.13.5 | htseq/py36/0.13 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 0.13.5 | htseq/py39/0.13 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 0.5.4p5 | htseq/0.5.4p5 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 0.6.1p1 | htseq/0.6.1p1 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 0.9.1 | htseq/0.9 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 2.0.5 | htseq/py39/2.0 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htseq | 2.0.5 | htseq/py310/2.0 | None | application | computational biology | HTSeq - Analysing high-throughput sequencing data with Python |
htslib | 1.12.2 | htslib/1.12 | compiler/intel/19 compiler/gcc/10 compiler/intel/20 compiler/gcc/9 | application | computational biology | HTSlib is an implementation of a unified C library for accessing common file formats. |
htslib | 1.3.2 | htslib/1.3 | None | application | computational biology | HTSlib is an implementation of a unified C library for accessing common file formats. |
htslib | 1.7 | htslib/1.7 | None | application | computational biology | HTSlib is an implementation of a unified C library for accessing common file formats. |
htstream | e919d21 | htstream/e919d21 | None | application | Bioinformatics | A toolset for high throughput sequence analysis using a streaming approach facilitated by Linux pipes. |
humann | 3.0.0 | humann/3.0 | None | application | computational biology | HUMAnN 3 is the next iteration of HUMAnN, the HMP Unified Metabolic Analysis Network. |
humann | 3.1.1 | humann/3.1 | None | application | computational biology | HUMAnN 3 is the next iteration of HUMAnN, the HMP Unified Metabolic Analysis Network. |
humann | 3.6 | humann/3.6 | None | application | computational biology | HUMAnN 3 is the next iteration of HUMAnN, the HMP Unified Metabolic Analysis Network. |
humann2 | 0.11.2 | humann2/0.11 | None | application | computational biology | HUMAnN2 is the HMP Unified Metabolic Analysis Network 2 |
humann2 | 0.9.9 | humann2/0.9 | None | application | computational biology | HUMAnN2 is the HMP Unified Metabolic Analysis Network 2 |
humann2 | 2.8.1 | humann2/2.8 | None | application | computational biology | HUMAnN2 is the HMP Unified Metabolic Analysis Network 2 |
i-pi | 2.4.0 | i-pi/py39/2.4 | None | application | molecular dynamics | i-PI: a universal force engine |
ibm-ilog-cplex | 12.10 | ibm-ilog-cplex/12.10 | None | application | iIBM ILOG CPLEX Optimization Studio | |
ibm-ilog-cplex | 20.10 | ibm-ilog-cplex/20.10 | None | application | iIBM ILOG CPLEX Optimization Studio | |
ibm-ilog-cplex | 22.1.0 | ibm-ilog-cplex/22.1.0 | None | application | iIBM ILOG CPLEX Optimization Studio | |
icount | 2.0.0 | icount/py36/2.0 | None | application | Bioinformatics | Computational pipeline for analysis of iCLIP data |
icount | 2.0.0 | icount/py37/2.0 | None | application | Bioinformatics | Computational pipeline for analysis of iCLIP data |
idba | 1.1.3 | idba/1.1 | None | application | computational biology | IDBA is a practical iterative De Bruijn Graph De Novo Assembler for sequence assembly in bioinfomatics. |
idr | 2.0 | idr/2.0 | None | application | computational biology | The IDR (Irreproducible Discovery Rate) framework is a unified approach to measure the reproducibility of findings identified from replicate experiments and provide highly stable thresholds based on reproducibility. |
igs-portal-client | 1.4.4 | igs-portal-client/1.4 | None | application | System | Python-based client for downloading data made available through portals powered by the GDC-based portal system. |
igvtools | 2.14.1 | igvtools/2.14 | None | application | genomics | Command line tools for IGV |
igvtools | 2.16.2 | igvtools/2.16 | None | application | genomics | Command line tools for IGV |
igvtools | 2.5.3 | igvtools/2.5 | None | application | genomics | Command line tools for IGV |
ilastik | 1.3.3post3 | ilastik/1.3 | None | application | Image Processing | ilastik is a gui driven open source interactive image classification, segmentation and analysis tool that uses machine learning. |
ilastik | 1.4.0.post1 | ilastik/1.4 | None | application | Image Processing | ilastik is a gui driven open source interactive image classification, segmentation and analysis tool that uses machine learning. |
ilastik-gpu | 1.4.0.post1 | ilastik-gpu/1.4 | None | application | Image Processing | ilastik is a gui driven open source interactive image classification, segmentation and analysis tool that uses machine learning. |
ima3 | 1.0 | ima3/1.0 | None | application | Phylogeny | IMa3 provides for estimation of the posterior probability of the population phylogenetic topology by using a new kind of data augmentation called a 'hidden genealogy'. |
imagemagick | 7.0.8_10 | imagemagick/7.0 | None | application | bitmap | Software suite to create, edit, compose, or convert bitmap images. |
imagemagick | 7.1.0_2 | imagemagick/7.1 | None | application | bitmap | Software suite to create, edit, compose, or convert bitmap images. |
imbalanced-learn-gpu | 0.4.3 | imbalanced-learn-gpu/py36/0.4 | None | application | Machine Learning | Python module to balance data set using under- and over-sampling |
imbalanced-learn-gpu | 0.4.3 | imbalanced-learn-gpu/py37/0.4 | None | application | Machine Learning | Python module to balance data set using under- and over-sampling |
impute2 | 2.3.2 | impute2/2.3 | None | application | computational biology | IMPUTE2 is a computer program for phasing observed genotypes and imputing missing genotypes. |
instrain | 1.3.7 | instrain/1.3 | None | application | bioinformatics | Calculation of strain-level metrics |
intel-mkl | 12 | intel-mkl/12 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 13 | intel-mkl/13 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 15 | intel-mkl/15 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 16 | intel-mkl/16 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 18 | intel-mkl/18 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 19 | intel-mkl/19 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 20 | intel-mkl/20 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 2021.1 | intel-mkl/2021.1 | None | library | tools | Numerical library, contains blas/lapack |
intel-mkl | 2022.0 | intel-mkl/2022.0 | None | library | tools | Numerical library, contains blas/lapack |
intel-mpi | 18 | intel-mpi/18 | compiler/intel/18 | library | runtime support | |
intel-mpi | 19 | intel-mpi/19 | compiler/intel/19 | library | runtime support | |
intel-mpi | 2021 | intel-mpi/2021 | compiler/intel/2021 | library | runtime support | |
intel-tbb | 2021.13 | intel-tbb/2021.13 | None | library | runtime support | |
intel-tbb | 2021.2 | intel-tbb/2021.2 | None | library | runtime support | |
intel-tbb | 2021.5 | intel-tbb/2021.5 | None | library | runtime support | |
interproscan | 5.52-86.0 | interproscan/5.52 | None | application | computational biology | Scans a range of protein signatures against your sequences and provides protein functional analysis. |
interproscan | 5.63-95.0 | interproscan/5.63 | None | application | computational biology | Scans a range of protein signatures against your sequences and provides protein functional analysis. |
interproscan | 5.69-101.0 | interproscan/5.69 | None | application | computational biology | Scans a range of protein signatures against your sequences and provides protein functional analysis. |
interproscan | 5.8-49.0 | interproscan/5.8 | None | application | computational biology | Scans a range of protein signatures against your sequences and provides protein functional analysis. |
ipr-support | 1.0 | ipr-support/1.0 | None | application | computational biology | Support environment containing a few small libraries for InterProScan. Not useful as a stand-alone environment. |
iqtree | 1.6.7 | iqtree/1.6 | None | application | computational biology | IQ-TREE creates phylogenetic trees under maximum likelihood with emphasis on speed and accuracy. |
iqtree | 2.2.2.7 | iqtree/2.2 | None | application | computational biology | IQ-TREE creates phylogenetic trees under maximum likelihood with emphasis on speed and accuracy. |
iqtree | 2.3.4 | iqtree/2.3 | None | application | computational biology | IQ-TREE creates phylogenetic trees under maximum likelihood with emphasis on speed and accuracy. |
irods | 4.1 | irods/4.1 | None None | application | unknown | The integrated Rule-Oriented Data System (iRODS) is open source data management software used by research organizations and government agencies worldwide. This module includes the icommands client programs only. |
irods | 4.2 | irods/4.2 | None | application | unknown | The integrated Rule-Oriented Data System (iRODS) is open source data management software used by research organizations and government agencies worldwide. This module includes the icommands client programs only. |
itk | 5.2.0 | itk/py37/5.2 | None | application | Utility | ITK is an open-source toolkit for multidimensional image analysis |
itk | 5.2.0 | itk/py38/5.2 | None | application | Utility | ITK is an open-source toolkit for multidimensional image analysis |
itk | 5.2.0 | itk/py39/5.2 | None | application | Utility | ITK is an open-source toolkit for multidimensional image analysis |
ivar | 1.4.2 | ivar/1.4 | None | application | computational biology | iVar is a computational package that contains functions broadly useful for viral amplicon-based sequencing. |
jags | 4.3 | jags/4.3 | compiler/intel/2021 compiler/gcc/11 | application | mathematics | JAGS is Just Another Gibbs Sampler. |
jamm | 1.0.7r2 | jamm/1.0.7r2 | None | application | computational biology | JAMM is a peak finder for NGS datasets (ChIP-Seq, ATAC-Seq, DNase-Seq..etc.) that can integrate replicates and assign peak boundaries accurately. |
jasper | 1.9 | jasper/1.9 | compiler/pgi/20 | library | runtime support | A reference implementation of the codec specified in the JPEG-2000 Part-1 standard. |
jasper | 1.900.22 | jasper/1.900.22 | compiler/pgi/20 | library | runtime support | A reference implementation of the codec specified in the JPEG-2000 Part-1 standard. |
jasper | 2.0 | jasper/2.0 | compiler/pgi/20 compiler/intel/20 compiler/gcc/10 compiler/intel/19 compiler/gcc/9 | library | runtime support | A reference implementation of the codec specified in the JPEG-2000 Part-1 standard. |
jasper | 4.0.0 | jasper/4.0 | None | library | runtime support | A reference implementation of the codec specified in the JPEG-2000 Part-1 standard. |
java | 1.6 | java/1.6 | None | application | system | OpenJDK (Java). |
java | 1.7 | java/1.7 | None | application | system | OpenJDK (Java). |
java | 1.8 | java/1.8 | None | application | system | OpenJDK (Java). |
java | 11 | java/11 | None | application | system | OpenJDK (Java). |
java | 12 | java/12 | None | application | system | OpenJDK (Java). |
java | 17 | java/17 | None | application | system | OpenJDK (Java). |
java | 19 | java/19 | None | application | system | OpenJDK (Java). |
jellyfish | 2.2.0 | jellyfish/2.2 | None | application | Biology | Jellyfish is a tool for fast, memory-efficient counting of k-mers in DNA. A k-mer is a substring of length k, and counting the occurrences of all such substrings is a central step in many analyses of DNA sequence |
jellyfish | 2.3.0 | jellyfish/2.3 | None | application | Biology | Jellyfish is a tool for fast, memory-efficient counting of k-mers in DNA. A k-mer is a substring of length k, and counting the occurrences of all such substrings is a central step in many analyses of DNA sequence |
jmosaics | 1.10 | jmosaics/1.10 | None | application | computational biology | Joint analysis of multiple ChIP-Seq data sets. |
jpeg | 9e | jpeg/9e | compiler/pgi/20 compiler/gcc/11 compiler/intel/19 compiler/gcc/9 compiler/intel/20 compiler/gcc/10 | library | runtime support | |
jq | 1.6 | jq/1.6 | None | application | Utility | A command-line JSON processor. |
juicer | 1.6 | juicer/1.6 | None | application | computational biology | A One-Click System for Analyzing Loop-Resolution Hi-C Experiments. |
julia | 0.6.2 | julia/0.6 | None | application | Language | A high-performance dynamic programming language for data science |
julia | 1.0 | julia/1.0 | None | application | Language | A high-performance dynamic programming language for data science |
julia | 1.1.1 | julia/1.1 | None | application | Language | A high-performance dynamic programming language for data science |
julia | 1.10.2 | julia/1.10 | None | application | Language | A high-performance dynamic programming language for data science |
julia | 1.6.1 | julia/1.6 | None | application | Language | A high-performance dynamic programming language for data science |
julia | 1.7.2 | julia/1.7 | None | application | Language | A high-performance dynamic programming language for data science |
julia | 1.9.2 | julia/1.9 | None | application | Language | A high-performance dynamic programming language for data science |
jupyter-book | 0.15.1 | jupyter-book/0.15 | None | application | Publishing | Jupyter Book: Create an online book with Jupyter Notebooks |
justorthologs | 0.0.20190308 | justorthologs/0.0.20190308 | None | application | Biology | JustOrthologs: a fast, accurate and user-friendly ortholog identification algorithm. |
jvarkit | 2024.04.20 | jvarkit/2024.04.20 | None | application | bioinformatics Java | Java utilities for Bioinformatics. |
jvarkit-msa2vcf | 1.0 | jvarkit-msa2vcf/1.0 | None | application | computational biology | Getting a VCF file from a CLUSTAW or a FASTA alignment. |
jvarkit-sam2tsv | 1.0 | jvarkit-sam2tsv/1.0 | None | application | computational biology | Prints the SAM alignments as a TAB delimited file. |
jvarkit-vcf2bam | 2018.04.05 | jvarkit-vcf2bam/2018.04.05 | None | application | computational biology | Converts VCF to BAM files |
jwt-cli | 3.3.0 | jwt-cli/3.3 | None | application | json | A super fast CLI tool to decode and encode JWTs built in Rust. |
kaiju | 1.10.0 | kaiju/1.10 | None | application | Bioinformatics | Fast and sensitive taxonomic classification for metagenomics |
kaiju | 1.7.3 | kaiju/1.7 | None | application | Bioinformatics | Fast and sensitive taxonomic classification for metagenomics |
kaiju | 1.8.2 | kaiju/1.8 | None | application | Bioinformatics | Fast and sensitive taxonomic classification for metagenomics |
kalign | 2.0 | kalign/2.0 | None | application | computational biology | Kalign is a fast and accurate multiple sequence alignment algorithm designed to align large numbers of protein sequences. |
kalign | 2.03 | kalign/2.03 | None | application | computational biology | Kalign is a fast and accurate multiple sequence alignment algorithm designed to align large numbers of protein sequences. |
kallisto | 0.46.2 | kallisto/0.46 | None | application | computational biology | Kallisto is a program for quantifying abundances of transcripts from bulk and single-cell RNA-Seq data, or more generally of target sequences using high-throughput sequencing reads. It is based on the novel idea of pseudoalignment for rapidly determining the compatibility of reads with targets, without the need for alignment. |
kat | 2.4.0 | kat/2.4 | None | application | bioinformatics | KAT is a suite of tools that analyse jellyfish hashes or sequence files (fasta or fastq) using kmer counts |
keras | 2.2.4 | keras/py27/2.2 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras | 2.2.4 | keras/py36/2.2 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras | 2.3.1 | keras/py27/2.3 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras | 2.3.1 | keras/py36/2.3 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras | 2.4.3 | keras/py37/2.4 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras | 2.4.3 | keras/py38/2.4 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras | 2.6.0 | keras/py38/2.6 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras | 2.6.0 | keras/py39/2.6 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.2.4 | keras-gpu/py27/2.2 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.2.4 | keras-gpu/py36/2.2 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.3.1 | keras-gpu/py27/2.3 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.3.1 | keras-gpu/py36/2.3 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.4.3 | keras-gpu/py37/2.4 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.4.3 | keras-gpu/py38/2.4 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.6.0 | keras-gpu/py38/2.6 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
keras-gpu | 2.6.0 | keras-gpu/py39/2.6 | None | application | machine learning | Deep Learning Library for Theano and TensorFlow |
khmer | 2.0 | khmer/2.0 | None | application | computational biology | Khmer is tools for in-memory nucleotide sequence k-mer counting, filtering, graph traversal and more. |
kmc | 3.1.1 | kmc/3.1 | None | application | computational biology | Tools for efficient k-mer counting and filtering of reads based on k-mer content |
kneaddata | 0.10.0 | kneaddata/0.10 | None | application | computational biology | KneadData is a tool designed to perform quality control on metagenomic and metatranscriptomic sequencing data, especially data from microbiome experiments. |
kneaddata | 0.12.0 | kneaddata/0.12 | None | application | computational biology | KneadData is a tool designed to perform quality control on metagenomic and metatranscriptomic sequencing data, especially data from microbiome experiments. |
kneaddata | 0.7.2 | kneaddata/0.7 | None | application | computational biology | KneadData is a tool designed to perform quality control on metagenomic and metatranscriptomic sequencing data, especially data from microbiome experiments. |
kraken | 1.0 | kraken/1.0 | None | application | computational biology | Kraken is a system for assigning taxonomic labels to short DNA sequences, usually obtained through metagenomic studies. |
kraken2 | 2.0.8-beta | kraken2/2.0.8-beta | None | application | Bioinformatics | Kraken is a system for assigning taxonomic labels to short DNA sequences, usually obtained through metagenomic studies. |
kraken2 | 2.1.3 | kraken2/2.1 | None | application | Bioinformatics | Kraken is a system for assigning taxonomic labels to short DNA sequences, usually obtained through metagenomic studies. |
krona | 2.7.1 | krona/2.7 | None | application | bioinformatics | Krona Tools is a set of scripts to create Krona charts from several Bioinformatics tools as well as from text and XML files. |
kronos | 2.3.0 | kronos/2.3 | None | application | workflow | Kronos is a highly flexible Python-based software tool that mainly enables bioinformatics developers, i.e. bioinformaticians who develop workflows for analyzing genomic data, to quickly make a workflow. |
ksnp | 3.1 | ksnp/3.1 | None | application | computational biology | kSNP identifies the pan-genome SNPs in a set of genome sequences, and estimates phylogenetic trees based upon those SNPs. |
lammps | 07Aug2019 | lammps/07Aug2019 | compiler/gcc/11:openmpi/4.1 | library | runtime support | |
lammps | 23Jun2022 | lammps/23June2022 | compiler/gcc/11:openmpi/4.1 | library | runtime support | |
lammps | 27June2024 | lammps/27June2024 | compiler/intel/20:openmpi/4.1 compiler/gcc/11:openmpi/4.1 | library | runtime support | |
lammps | 29Sep2021 | lammps/29Sep2021 | compiler/gcc/11:openmpi/4.1 compiler/gcc/10:openmpi/4.0 compiler/intel/20:openmpi/4.1 compiler/intel/19:openmpi/4.0 compiler/gcc/10:openmpi/4.1 | library | runtime support | |
lammps | 2Aug2023 | lammps/2Aug2023 | compiler/gcc/11:openmpi/4.1 compiler/intel/20:openmpi/4.1 | library | runtime support | |
lapack | 3.9.1 | lapack/3.9 | compiler/intel/18 compiler/intel/20 compiler/gcc/9 compiler/gcc/11 compiler/gcc/10 compiler/pgi/20 compiler/intel/19 | application | Utility | LAPACK is written in Fortran 90 and provides routines for solving systems of simultaneous linear equations, least-squares solutions of linear systems of equations, eigenvalue problems, and singular value problems. |
lasagne | 0.1 | lasagne/py27/0.1 | None | application | neural networks | A lightweight library to build and train neural networks in Theano |
lasagne | 0.1 | lasagne/py36/0.1 | None | application | neural networks | A lightweight library to build and train neural networks in Theano |
lastools | v2.0.2 | lastools/2.0 | None | application | Geoscience | LASlib and LASzip libraries plus open source utilities from LAStools for manipulating LiDAR data in LAS format |
lastz | 1.04.22 | lastz/1.04 | None | application | computational biology | LASTZ is a program for aligning DNA sequences, a pairwise aligner. |
lcms2 | 2.13.1 | lcms2/2.13 | compiler/intel/20 compiler/pgi/20 compiler/intel/19 compiler/gcc/9 compiler/gcc/10 | library | runtime support | |
lefse | 1.0.8.post1 | lefse/1.0 | None | application | computational biology | LEfSe (Linear discriminant analysis Effect Size) determines the features (organisms, clades, operational taxonomic units, genes, or functions) most likely to explain differences between classes by coupling standard tests for statistical significance with additional tests encoding biological consistency and effect relevance. |
lefse | 1.1.2 | lefse/1.1 | None | application | computational biology | LEfSe (Linear discriminant analysis Effect Size) determines the features (organisms, clades, operational taxonomic units, genes, or functions) most likely to explain differences between classes by coupling standard tests for statistical significance with additional tests encoding biological consistency and effect relevance. |
lftp | 4.8.3 | lftp/4.8 | None | application | system | LFTP is a sophisticated file transfer program supporting a number of network protocols (ftp, http, sftp, fish, torrent). |
lftp | 4.9.1 | lftp/4.9 | None | application | system | LFTP is a sophisticated file transfer program supporting a number of network protocols (ftp, http, sftp, fish, torrent). |
libbeef | 0.1.3 | libbeef/0.1 | compiler/intel/19 compiler/gcc/9 compiler/intel/20 compiler/pgi/20 compiler/gcc/10 | application | Physics | |
libgeotiff | 1.6.0 | libgeotiff/1.6 | compiler/intel/19 compiler/gcc/10 compiler/intel/20 compiler/gcc/9 compiler/pgi/20 | library | runtime support | |
libidn | 1.36 | libidn/1.36 | compiler/intel/19 | library | runtime support | |
libint | 2.6.0 | libint/2.6 | compiler/intel/20 | library | runtime support | |
libjpeg | 2.0.5 | libjpeg/2.0 | compiler/pgi/20 compiler/gcc/11 compiler/gcc/9 compiler/gcc/10 compiler/intel/20 compiler/intel/19 | library | runtime support | |
libpng | 1.6.37 | libpng/1.6 | compiler/pgi/20 compiler/gcc/10 compiler/gcc/11 compiler/intel/19 compiler/intel/20 compiler/gcc/9 | library | runtime support | |
libtiff | 4.1.0 | libtiff/4.1 | compiler/gcc/11 compiler/gcc/9 compiler/intel/19 compiler/gcc/10 compiler/pgi/20 compiler/intel/20 | library | runtime support | |
libwebp | 1.1.0 | libwebp/1.1 | compiler/intel/19 compiler/gcc/10 compiler/pgi/20 compiler/intel/20 compiler/gcc/11 compiler/gcc/9 | library | runtime support | |
libxc | 5.1.6 | libxc/5.1 | compiler/intel/20 compiler/pgi/20 compiler/gcc/10 compiler/intel/19 compiler/gcc/9 | library | runtime support | |
libxc | 5.2.0 | libxc/5.2 | compiler/gcc/9 compiler/gcc/10 compiler/intel/20 compiler/pgi/20 compiler/intel/19 | library | runtime support | |
libxml2 | 2.9.9 | libxml2/2.9 | compiler/intel/20 compiler/intel/18 compiler/pgi/20 compiler/intel/19 compiler/gcc/10 compiler/gcc/9 | library | runtime support | |
libxsmm | 1.17 | libxsmm/1.17 | compiler/intel/20 | library | runtime support | |
lmdb | 0.9 | lmdb/0.9 | None | library | unknown | Lightning memory-mapped database library. |
lmod | None | lmod | None | unknown | unknown | Lmod: An Environment Module System |
lmod | lmod | lmod/lmod | None | unknown | unknown | Lmod: An Environment Module System |
lofreq | 2.1.3.1 | lofreq/2.1 | None | application | computational biology | LoFreq is a fast and sensitive variant-caller for inferring SNVs and indels from next-generation sequencing data. |
logomaker | 0.8 | logomaker/py27/0.8 | None | application | Utility | Package for making Sequence Logos |
logomaker | 0.8 | logomaker/py36/0.8 | None | application | Utility | Package for making Sequence Logos |
ls-bsr | 0.0.2022.11.15 | ls-bsr/2022.11.15 | None | application | bioinformatics | Large scale Blast Score Ratio (BSR) analysis. |
lsdyna | 12.0.0 | lsdyna/12 | None | unknown | unknown | |
lsdyna | 13.1.1 | lsdyna/13.1 | None | unknown | unknown | |
lsdyna | 14.0.0 | lsdyna/14.0 | None | unknown | unknown | |
lynx | 2.8.8 | lynx/2.8 | None | application | tool | Lynx is a text browser for the World Wide Web. |
lyve-set | 2.0.1 | lyve-set/2.0 | None | application | computational biology | LYVE version of the Snp Extraction Tool (SET), a method of using hqSNPs to create a phylogeny. |
m4 | 1.0 | m4/1.4 | None | application | Utilities | The autotools collection is a set of tools that make it easy to build and install programs from a source distribution. |
maaslin | 0.0.5 | maaslin/0.05 | None | application | computational biology | MaAsLin is a multivariate statistical framework that finds associations between clinical metadata and microbial community abundance or function. |
maaslin2 | 0.3.0 | maaslin2/0.3 | None | application | computational biology | MaAsLin2 is comprehensive R package for efficiently determining multivariable association between microbial meta'omic features and clinical metadata. |
maaslin2 | 0.99.12 | maaslin2/0.99 | None | application | computational biology | MaAsLin2 is comprehensive R package for efficiently determining multivariable association between microbial meta'omic features and clinical metadata. |
macs2 | 2.1.1 | macs2/2.1 | None | application | computational biology | MACS -- Model-based Analysis of ChIP-Seq |
macs2 | 2.2.9 | macs2/2.2 | None | application | computational biology | MACS -- Model-based Analysis of ChIP-Seq |
macs3 | 3.0.2 | macs3/3.0 | None | application | computational biology | MACS -- Model-based Analysis of ChIP-Seq |
maestro | 1.5.1 | maestro/1.5 | None | application | computational biology | MAESTRO(Model-based AnalysEs of Single-cell Transcriptome and RegulOme) is a comprehensive single-cell RNA-seq and ATAC-seq analysis suit built using snakemake. |
mafft | 7.149 | mafft/7.149 | None | application | Bioinformatics | Multiple alignment program for amino acid or nucleotide sequences based on fast Fourier transform |
mafft | 7.407 | mafft/7.407 | None | application | Bioinformatics | Multiple alignment program for amino acid or nucleotide sequences based on fast Fourier transform |
mafft | 7.520 | mafft/7.520 | None | application | Bioinformatics | Multiple alignment program for amino acid or nucleotide sequences based on fast Fourier transform |
mafft | 7.526 | mafft/7.526 | None | application | Bioinformatics | Multiple alignment program for amino acid or nucleotide sequences based on fast Fourier transform |
magicblast | 1.7.0 | magicblast/1.7 | None | application | computational biology | NCBI BLAST next generation read mapper |
make | 1.0 | make/4.3 | None | application | Utilities | The autotools collection is a set of tools that make it easy to build and install programs from a source distribution. |
maker | 2.31.10 | maker/2.31 | None | application | computational biology | MAKER is a genome annotation pipeline for prokaryotic and smaller eukaryotic organisms. |
maker | 3.01.03 | maker/3.01 | None | application | computational biology | MAKER is a genome annotation pipeline for prokaryotic and smaller eukaryotic organisms. |
mamba | 0.13.0 | mamba/0.13 | None | application | system | |
mamba | 0.15.3 | mamba/0.15 | None | application | system | |
mamba | 0.5.1 | mamba/0.5.1 | None | application | system | |
mamba | 0.7.3 | mamba/0.7 | None | application | system | |
mamba | 23.1.0/1.3.1 | mamba/1.3 | None | application | system | |
mamba | 23.11.0/1.5.4 | mamba/1.5 | None | application | system | |
mamba | 23.7.2/1.4.9 | mamba/1.4 | None | application | system | |
mamba | 4.12.0/0.24.0 | mamba/0.24 | None | application | system | |
manta | 1.6.0 | manta/1.6 | None | application | Structural variant | Structural variant and indel caller for mapped sequencing data |
mapping-iterative-assembler | 1.0 | mapping-iterative-assembler/1.0 | None | application | bioinformatics | Consensus calling or `reference assisted assembly`, chiefly of ancient mitochondria. |
mapsplice | 2.2.0 | mapsplice/2.2 | None | application | computational biology | MapSplice is a software for mapping RNA-seq data to reference genome for splice junction discovery that depends only on reference genome, and not on any further annotations. |
maq | 0.7 | maq/0.7 | None | application | computational biology | maq - Mapping and Assembly with Quality. |
mash | 2.2.2 | mash/2.2 | None | application | computational biology | Fast sequence distance estimator that uses MinHash |
mashmap | 2.0 | mashmap/2.0 | None | application | computational biology | A fast approximate aligner for long DNA sequences |
mashmap | 3.1.1 | mashmap/3.1 | None | application | computational biology | A fast approximate aligner for long DNA sequences |
mashtree | 1.4.6 | mashtree/1.4 | None | application | computational biology | Create a tree using Mash distances |
masurca | 3.3.1 | masurca/3.3 | None | application | Biology | MaSuRCA (Maryland Super-Read Celera Assembler) genome assembly software. MaSuRCA requires Illumina data, and supports third-generation PacBio/Nanopore MinION reads for hybrid assembly. |
masurca | 4.0.9 | masurca/4.0 | None | application | Biology | MaSuRCA (Maryland Super-Read Celera Assembler) genome assembly software. MaSuRCA requires Illumina data, and supports third-generation PacBio/Nanopore MinION reads for hybrid assembly. |
masurca | 4.1.0 | masurca/4.1 | None | application | Biology | MaSuRCA (Maryland Super-Read Celera Assembler) genome assembly software. MaSuRCA requires Illumina data, and supports third-generation PacBio/Nanopore MinION reads for hybrid assembly. |
mathematica | 11.0 | mathematica/11.0 | None | application | Engineering | |
mathematica | 11.3 | mathematica/11.3 | None | application | Engineering | |
mathematica | 12.0 | mathematica/12.0 | None | application | Engineering | |
mathematica | 12.3 | mathematica/12.3 | None | application | Engineering | |
mathematica | 13.1 | mathematica/13.1 | None | application | Engineering | |
mathematica | 13.2 | mathematica/13.2 | None | application | Engineering | |
matio | 1.5 | matio/1.5 | compiler/gcc/10 | library | runtime support | |
matlab | r2012b | matlab/r2012b | None | unknown | unknown | |
matlab | r2013b | matlab/r2013b | None | unknown | unknown | |
matlab | r2014b | matlab/r2014b | None | unknown | unknown | |
matlab | r2015b | matlab/r2015b | None | unknown | unknown | |
matlab | r2016a | matlab/r2016a | None | unknown | unknown | |
matlab | r2016b | matlab/r2016b | None | unknown | unknown | |
matlab | r2017a | matlab/r2017a | None | unknown | unknown | |
matlab | r2017b | matlab/r2017b | None | unknown | unknown | |
matlab | r2018a | matlab/r2018a | None | unknown | unknown | |
matlab | r2018b | matlab/r2018b | None | unknown | unknown | |
matlab | r2019a | matlab/r2019a | None | unknown | unknown | |
matlab | r2019b | matlab/r2019b | None | unknown | unknown | |
matlab | r2020a | matlab/r2020a | None | unknown | unknown | |
matlab | r2020b | matlab/r2020b | None | unknown | unknown | |
matlab | r2021a | matlab/r2021a | None | unknown | unknown | |
matlab | r2021b | matlab/r2021b | None | unknown | unknown | |
matlab | r2022a | matlab/r2022a | None | unknown | unknown | |
matlab | r2022b | matlab/r2022b | None | unknown | unknown | |
matlab | r2023a | matlab/r2023a | None | unknown | unknown | |
matlab | r2023b | matlab/r2023b | None | unknown | unknown | |
matlab | r2024a | matlab/r2024a | None | unknown | unknown | |
mauve | 2.4 | mauve/2.4 | None | application | computational biology | mauve - Multiple Genome Alignment. |
maven | 3.2 | maven/3.2 | None | application | system | Apache Maven is a software project management and comprehension tool. |
maven | 3.5 | maven/3.5 | None | application | system | Apache Maven is a software project management and comprehension tool. |
maxbin2 | 2.2.7 | maxbin2/2.2 | None | application | Biology | MaxBin is software for binning assembled metagenomic sequences based on an Expectation-Maximization algorithm. |
maxquant | 1.6.10.43 | maxquant/1.6 | None | application | biochemistry | MaxQuant is a quantitative proteomics software package designed for analyzing large mass-spectrometric data sets. License restricted. |
maxquant | 2.0.3.0 | maxquant/2.0 | None | application | biochemistry | MaxQuant is a quantitative proteomics software package designed for analyzing large mass-spectrometric data sets. License restricted. |
mbuffer | 20171011 | mbuffer/20171011 | None | application | buffer | Mbuffer is a tool for buffering data streams with a large set of unique features. |
mcl | 14.137 | mcl/14.137 | None | application | computational biology | MCL |
medaka | 1.7.2 | medaka/py38/1.7 | None | application | bioinformatics | Neural network sequence error correction. |
medaka-gpu | 1.7.2 | medaka-gpu/py38/1.7 | None | application | bioinformatics | Neural network sequence error correction. |
meep | 1.3 | meep/1.3 | None | library | runtime support | |
meerkat | 0.189 | meerkat/0.1 | None | application | computational biology | Meerkat is designed to identify structural variations |
megahit | 1.1 | megahit/1.1 | None | application | computational biology | MEGAHIT: An ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph |
megahit | 1.2.9 | megahit/1.2 | None | application | computational biology | MEGAHIT: An ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph |
megahit-gpu | 1.1 | megahit-gpu/1.1 | None | application | computational biology | MEGAHIT: An ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph. |
megalodon | 2.4.1 | megalodon/2.4 | None | application | Genomics | Nanopore modified base and sequence variant detection. |
megalodon | 2.5.0 | megalodon/2.5 | None | application | Genomics | Nanopore modified base and sequence variant detection. |
megalodon-gpu | 2.5.0 | megalodon-gpu/2.5 | None | application | Bioinformatics | Nanopore modified base and sequence variant detection. |
megan | 6.12.3 | megan/6.12 | None | application | Computational Biology | A tool for studying the taxonomic content of a set of DNA reads |
megan | 6.25.9 | megan/6.25 | None | application | Computational Biology | A tool for studying the taxonomic content of a set of DNA reads |
melonnpan | 2019.03.22 | melonnpan/2019.03.22 | None | application | computational biology | MelonnPan is a computational method for predicting metabolite compositions from shotgun metagenomic sequencing data. |
merqury | 1.3 | merqury/1.3 | None | application | Genome Analysis | Evaluate genome assemblies with k-mers and more. |
meryl | 1.4.1 | meryl/1.4 | None | application | genome analysis | A genomic k-mer counter (and sequence utility) with nice features |
meson | 0.61.1 | meson/0.61 | None | application | Utilities | The Meson Build System |
metabat2 | 2.15 | metabat2/2.15 | None | application | computational biology | Metagenome binning |
metabolic | 20210303 | metabolic/20210303 | None | application | Bioinformatics | A scalable high-throughput metabolic and biogeochemical functional trait profiler. |
metacv | 2.3.0 | metacv/2.3 | None | application | Bioinformatics | Composition based classification for short metagenomic sequences |
metaphlan | 1.7 | metaphlan/1.7 | None | application | metagenomic phylogenetic analysis | MetaPhlAn is a computational tool for profiling the composition of microbial communities from metagenomic shotgun sequencing data. |
metaphlan | 3.0.3 | metaphlan/3.0 | None | application | metagenomic phylogenetic analysis | MetaPhlAn is a computational tool for profiling the composition of microbial communities from metagenomic shotgun sequencing data. |
metaphlan | 3.1.0 | metaphlan/3.1 | None | application | metagenomic phylogenetic analysis | MetaPhlAn is a computational tool for profiling the composition of microbial communities from metagenomic shotgun sequencing data. |
metaphlan | 4.0.6 | metaphlan/4.0 | None | application | metagenomic phylogenetic analysis | MetaPhlAn is a computational tool for profiling the composition of microbial communities from metagenomic shotgun sequencing data. |
metaphlan2 | 2.6.0 | metaphlan2/2.6 | None | application | metagenomic phylogenetic analysis | MetaPhlAn is a computational tool for profiling the composition of microbial communities from metagenomic shotgun sequencing data. |
metaphlan2 | 2.7.8 | metaphlan2/2.7 | None | application | metagenomic phylogenetic analysis | MetaPhlAn is a computational tool for profiling the composition of microbial communities from metagenomic shotgun sequencing data. |
metaphlan2 | 2.96.1 | metaphlan2/2.96 | None | application | metagenomic phylogenetic analysis | MetaPhlAn is a computational tool for profiling the composition of microbial communities from metagenomic shotgun sequencing data. |
metasnv | 2.0.1 | metasnv/2.0 | None | application | Biology | SNV calling software |
metasv | 0.5.4 | metasv/0.5 | None | application | computational biology | An accurate and integrative structural-variant caller for next generation sequencing. |
metavelvet | 1.2.01 | metavelvet/1.2 | None | application | computational biology | MetaVelvet is an extension of Velvet assembler to de novo metagenome assembly from short sequence reads. |
metawrap | 1.1 | metawrap/1.1 | None | application | computational biology | MetaWRAP is a pipeline for genome-resolved metagenomic data analysis |
metawrap | 1.2 | metawrap/1.2 | None | application | computational biology | MetaWRAP is a pipeline for genome-resolved metagenomic data analysis |
metawrap | 1.3.2 | metawrap/1.3 | None | application | computational biology | MetaWRAP is a pipeline for genome-resolved metagenomic data analysis |
metaxa2 | 2.2.3 | metaxa2/2.2 | None | application | classification | Improved Identification and Taxonomic Classification of Small and Large Subunit rRNA in Metagenomic Data. |
methylpy | 1.4.1 | methylpy/py27/1.4 | None | application | bioinformatics | Bisulfite sequencing data processing and differential methylation analysis |
methylpy | 1.4.1 | methylpy/py36/1.4 | None | application | bioinformatics | Bisulfite sequencing data processing and differential methylation analysis |
methylpy | 1.4.1 | methylpy/py37/1.4 | None | application | bioinformatics | Bisulfite sequencing data processing and differential methylation analysis |
metis | 4.0.0 | metis/4.0 | compiler/gcc/9 | library | runtime support | |
metis | 5.1.0 | metis/5.1 | compiler/gcc/9 compiler/pgi/20 compiler/intel/19 compiler/intel/20 compiler/gcc/10 | library | runtime support | |
mfold | 3.6 | mfold/3.6 | None | application | computational biology | Mfold web server for nucleic acid folding and hybridization prediction. |
mgblast | 2.2.14 | mgblast/2.2 | None | application | Alignment | fast all-vs-all DNA alignment tool, modification of megablast from a 2006 version of NCBI C Toolkit |
mgltools | 1.5.7 | mgltools/1.5 | None | application | computational structural biology | MGLTools is an program for visualization and analisys of molecular structures. |
miRDeep | 2.0.0 | miRDeep/2.0 | None | application | computational biology | miRDeep2 is a completely overhauled tool which discovers microRNA genes by analyzing sequenced RNAs. |
micropita | 1.1.0 | micropita/1.1 | None | application | computational biology | microPITA is a computational tool enabling sample selection in two-stage (tiered) studies. |
midas | 1.3.2 | midas/1.3 | None | application | computational biology | An integrated pipeline for estimating strain-level genomic variation from metagenomic data |
midnight-commander | 4.8.22 | midnight-commander/4.8 | None | application | Utility | GNU Midnight Commander is a visual file manager, licensed under GNU General Public License and therefore qualifies as Free Software. It's a feature rich full-screen text mode application that allows you to copy, move and delete files and whole directory trees, search for files and run commands in the subshell. Internal viewer and editor are included. |
minibusco | 0.2.1 | minibusco/0.2 | None | application | bioinformatics | minibusco: a faster and more accurate reimplementation of BUSCO |
miniforge | 24.5.0/1.5.8 | miniforge/24.5 | None | application | system | |
minimap2 | 2.16 | minimap2/2.16 | None | application | bioinformatics | A versatile pairwise aligner for genomic and spliced nucleotide sequences. |
minimap2 | 2.26 | minimap2/2.26 | None | application | bioinformatics | A versatile pairwise aligner for genomic and spliced nucleotide sequences. |
minpack | 19961126 | minpack/19961126 | compiler/gcc/9 compiler/intel/20 compiler/pgi/20 compiler/gcc/10 compiler/intel/19 | application | Utility | Minpack includes software for solving nonlinear equations and nonlinear least squares problems. |
miranda | 3.3a | miranda/3.3a | None | application | computational biology | An algorithm for finding genomic targets for microRNAs |
misis | 1.0 | misis/1.0 | None | application | computational biology | |
mitosalt | 1.1.1 | mitosalt/1.1 | None | application | computational biology | Identification of mitochondrial structural alterations. |
mitoz | 3.6 | mitoz/3.6 | None | application | computational biology | MitoZ: A toolkit for assembly, annotation, and visualization of animal mitochondrial genomes |
mldata | 1.0 | mldata/1.0 | None | application | computer science | Static data resources for machine-learning/AI. |
mlflow | 2.16.2 | mlflow/py310/2.16 | None | application | machine learning | MLflow is an open source platform for the machine learning lifecycle. |
mlflow | 2.16.2 | mlflow/py312/2.16 | None | application | machine learning | MLflow is an open source platform for the machine learning lifecycle. |
mlpack | 2.2.5 | mlpack/2.2 | None | application | Machine Learning | mlpack a fast, flexible machine learning library |
mlpack | 3.0.3 | mlpack/3.0 | None | application | Machine Learning | mlpack a fast, flexible machine learning library |
mlst | 2.16.2 | mlst/2.16 | None | application | computational biology | Scan contig files against PubMLST typing schemes |
mlst | 2.19.0 | mlst/2.19 | None | application | computational biology | Scan contig files against PubMLST typing schemes |
mlst | 2.22.0 | mlst/2.22 | None | application | computational biology | Scan contig files against PubMLST typing schemes |
mmseqs2 | 13.45111 | mmseqs2/13.45111 | compiler/gcc/9:openmpi/4.0 compiler/gcc/10:openmpi/4.0 compiler/gcc/11:openmpi/4.1 | application | Bioinformatics | MMseqs2: ultra fast and sensitive search and clustering suite. |
modeller | 9.19 | modeller/9.19 | None | unknown | unknown | |
modflow-2005 | 1.12.00 | modflow-2005/1.12 | None | application | USGS | Three-dimensional finite-difference ground-water flow model. |
mongodb-client | 3.2 | mongodb-client/3.2 | None | application | Utility | Client programs for MongoDB. |
mongodb-client | 3.4 | mongodb-client/3.4 | None | application | Utility | Client programs for MongoDB. |
mongodb-client | 4.2 | mongodb-client/4.2 | None | application | Utility | Client programs for MongoDB. |
mono | 4.6 | mono/4.6 | None | application | compiler | Mono is a software platform designed to allow developers to easily create cross platform applications. |
mono | 5.10 | mono/5.10 | None | application | compiler | Mono is a software platform designed to allow developers to easily create cross platform applications. |
mono | 5.14.0.177 | mono/5.14 | None | application | compiler | Mono is a software platform designed to allow developers to easily create cross platform applications. |
morgan | 3.4 | morgan/3.4 | None | application | computational biology | MORGAN is part of our software for Markov chain Monte Carlo in Genetic Analysis. |
mosaik | 2.2 | mosaik/2.2 | None | application | computational biology | MOSAIK is a reference-guided aligner for next-generation sequencing technologies. |
mosdepth | 0.2.4 | mosdepth/0.2 | None | application | computational biology | Fast BAM/CRAM depth calculation for WGS, exome, or targetted sequencing. |
mosdepth | 0.3.8 | mosdepth/0.3 | None | application | computational biology | Fast BAM/CRAM depth calculation for WGS, exome, or targetted sequencing. |
mothur | 1.41.3 | mothur/1.41 | None | application | Bioinformatics | This project seeks to develop a single piece of open-source, expandable software to fill the bioinformatics needs of the microbial ecology community. |
mothur | 1.45.3 | mothur/1.45 | None | application | Bioinformatics | This project seeks to develop a single piece of open-source, expandable software to fill the bioinformatics needs of the microbial ecology community. |
mothur | 1.46.1 | mothur/1.46 | None | application | Bioinformatics | This project seeks to develop a single piece of open-source, expandable software to fill the bioinformatics needs of the microbial ecology community. |
mpfr | 4.1.0 | mpfr/4.1 | compiler/gcc/10 | library | runtime support | The MPFR library is a C library for multiple-precision floating-point computations with correct rounding. |
mpich | 3.4 | mpich/3.4 | compiler/gcc/9 | library | runtime support | |
mpich | 4.0 | mpich/4.0 | compiler/gcc/10 | library | runtime support | |
mpich2 | 1.5 | mpich2/1.5 | compiler/gcc/9 | library | runtime support | |
mplus | 6.12 | mplus/6.12 | None | application | unknown | Mplus is a latent variable modeling program with a wide variety of analysis capabilities. |
mplus | 7.0 | mplus/7.0 | None | application | unknown | Mplus is a latent variable modeling program with a wide variety of analysis capabilities. |
mrbayes | 3.2.7 | mrbayes/3.2 | None | application | computational biology | Bayesian Inference of Phylogeny |
mridata | 1.0 | mridata/1.0 | None | application | brain imaging | Static data resources for MRI/NeuroImaging. |
mrtrix3 | 3.0.3 | mrtrix3/3.0 | None | application | computational neuroimaging | Advanced tools for the analysis of diffusion MRI data. |
mrtrix3tissue | 5.2.9 | mrtrix3tissue/5.2 | None | application | computational neuroimaging | MRtrix3Tissue adds capabilities for 3-Tissue CSD modelling and analysis to a complete version of MRtrix3. |
msgf_plus | 2020.06.22 | msgf_plus/2020.06.22 | None | application | proteomics | MS-GF+ is a new MS/MS database search tool that is sensitive (it identifies more peptides than other database search tools and as many peptides as spectral library search tools) and universal (works well for diverse types of spectra, different configurations of MS instruments and different experimental protocols). |
mspkmercounter | 0.10.0 | mspkmercounter/0.10 | None | application | Biology | MSPKmerCounter is a k-mer counter based on the minimum substring partitioning technique. |
mugsy | 1.2.3 | mugsy/1.2 | None | application | computational biology | Mugsy is a multiple whole genome aligner. |
mujoco | 2.1.0 | mujoco/2.1 | None | application | Simulation | MuJoCo | advanced physics simulation. |
mujoco | 200 | mujoco/200 | None | application | Simulation | MuJoCo | advanced physics simulation. |
multigps | 0.74 | multigps/0.74 | None | application | computational biology | MultiGPS is a framework for analyzing collections of multi-condition ChIP-seq datasets and characterizing differential binding events between conditions. |
multiqc | 0.8 | multiqc/py27/0.8 | None | application | computational biology | MultiQC is a tool to create a single report with interactive plots for multiple bioinformatics analyses across many samples. |
multiqc | 0.8 | multiqc/py35/0.8 | None | application | computational biology | MultiQC is a tool to create a single report with interactive plots for multiple bioinformatics analyses across many samples. |
multiqc | 1.6 | multiqc/py27/1.6 | None | application | computational biology | MultiQC is a tool to create a single report with interactive plots for multiple bioinformatics analyses across many samples. |
multiqc | 1.6 | multiqc/py35/1.6 | None | application | computational biology | MultiQC is a tool to create a single report with interactive plots for multiple bioinformatics analyses across many samples. |
multiqc | 1.6 | multiqc/py36/1.6 | None | application | computational biology | MultiQC is a tool to create a single report with interactive plots for multiple bioinformatics analyses across many samples. |
multiqc | 1.8 | multiqc/py27/1.8 | None | application | computational biology | MultiQC is a tool to create a single report with interactive plots for multiple bioinformatics analyses across many samples. |
multiqc | 1.8 | multiqc/py37/1.8 | None | application | computational biology | MultiQC is a tool to create a single report with interactive plots for multiple bioinformatics analyses across many samples. |
multiwfn | 3.8 | multiwfn/3.8 | compiler/intel/18 | application | Wavefunction | Multiwfn is a powerful program for realizing electronic wavefunction analysis, which is a key ingredient of quantum chemistry. |
mumax3 | 3.10 | mumax3/3.10 | None | application | micromagnetics | GPU-accelerated micromagnetic simulator |
mumax3 | 3.9.3 | mumax3/3.9 | None | application | micromagnetics | GPU-accelerated micromagnetic simulator |
mummer | 3.23 | mummer/3.23 | None | application | bioinformatics | MUMmer is a system for rapidly aligning entire genomes |
mummer4 | 4.0.0beta2 | mummer4/4.0 | None | application | Bioinformatics | MUMmer is a system for rapidly aligning entire genomes |
muscle | 3.8.1551 | muscle/3.8 | None | application | computational biology | MUSCLE: multiple sequence alignment with high accuracy and high throughput |
muscle | 5.1 | muscle/5.1 | None | application | computational biology | MUSCLE: multiple sequence alignment with high accuracy and high throughput |
music | 1.0 | music/1.0 | None | application | computational biology | MUSIC is an algorithm for identification of enriched regions at multiple scales in the read depth signals from ChIP-Seq experiments. |
mutect | 1.1 | mutect/1.1 | None | application | computational biology | MuTect is a method developed at the Broad Institute for the reliable and accurate identification of somatic point mutations in next generation sequencing data of cancer genomes. |
mxnet | 0.9.3a | mxnet/0.9.3 | None | application | AI | MXNet is an open-source deep learning framework that allows you to define, train, and deploy deep neural networks on a wide array of devices, from cloud infrastructure to mobile devices. |
mxnet | 1.5.0 | mxnet/1.5 | None | application | AI | MXNet is an open-source deep learning framework that allows you to define, train, and deploy deep neural networks on a wide array of devices, from cloud infrastructure to mobile devices. |
mysql-client | 8.0.23 | mysql-client/8.0 | None | application | Database | MySQL client applications and tools |
mytaxa | 1.0 | mytaxa/1.0 | None | application | computational biology | MyTaxa - Assign taxonomy to metagenomic fragments. |
nano | 2.9.8 | nano/2.9 | None | application | Utility | Nano's ANOther editor, an enhanced free Pico clone |
nano | 5.5 | nano/5.5 | None | application | Utility | Nano's ANOther editor, an enhanced free Pico clone |
nano | 5.7 | nano/5.7 | None | application | Utility | Nano's ANOther editor, an enhanced free Pico clone |
nano | 6.2 | nano/6.2 | None | application | Utility | Nano's ANOther editor, an enhanced free Pico clone |
nano | 8.2 | nano/8.2 | None | application | Utility | Nano's ANOther editor, an enhanced free Pico clone |
nanofilt | 2.8.0 | nanofilt/2.8 | None | application | Bioinformatics | Filtering and trimming of Oxford Nanopore Sequencing data |
nanoplot | 1.40.2 | nanoplot/1.40 | None | application | computational biology | Plotting suite for long read sequencing data and alignments |
nanopolish | 0.14.0 | nanopolish/0.14 | None | application | bioinformatics | Signal-level algorithms for MinION data. |
ncbi-amrfinderplus | 3.8.4 | ncbi-amrfinderplus/3.8 | None | application | bioinformatics | AMRFinderPlus finds antimicrobial resistance and other genes in protein or nucleotide sequences. |
ncbi-datasets-cli | 16.4.4 | ncbi-datasets-cli/16.4 | None | application | bioinformatics | NCBI Datasets command-line clients |
ncbi-download | 0.2.6 | ncbi-download/0.2 | None | application | computational biology | Python scriopt for downloading bacterial and fungal genomes from NCBI. |
ncbi-download | 0.3.3 | ncbi-download/0.3 | None | application | computational biology | Python scriopt for downloading bacterial and fungal genomes from NCBI. |
ncdu | 1.15 | ncdu/1.15 | None | application | System | NCurses Disk Usage |
ncl | 6.6.2 | ncl/6.6 | None | application | utility | NCAR Command Language |
nco | 4.8.1 | nco/4.8 | None | library | runtime support | Suite of programs for manipulating NetCDF/HDF4 files. |
ncview | 2.1.7 | ncview/2.1 | compiler/pgi/20 compiler/intel/20 | library | runtime support | Ncview is a visual browser for netCDF format files. |
nda-tools | 0.2.23 | nda-tools/0.2 | None | application | NDA web services | Python package for interacting with NDA web services. |
neper | 3.3.0 | neper/3.3 | None | application | Applications | Neper is a software package for polycrystal generation and meshing. |
neper | 3.5.2 | neper/3.5 | None | application | Applications | Neper is a software package for polycrystal generation and meshing. |
neptune | 1.2.5 | neptune/1.2 | None | application | computational biology | Neptune locates genomic signatures using an exact k-mer matching strategy while accommodating k-mer mismatches. |
netcdf | 4.2 | netcdf/4.2 | compiler/intel/18 | library | runtime support | |
netcdf | 4.4 | netcdf/4.4 | compiler/gcc/9 | library | runtime support | |
netcdf | 4.4.0 | netcdf/4.4 | compiler/intel/18 | library | runtime support | |
netcdf | 4.5.0 | netcdf/4.5 | compiler/intel/20 compiler/gcc/9 compiler/gcc/10 compiler/intel/19 | library | runtime support | |
netcdf | 4.7 | netcdf/4.7 | compiler/pgi/20 | library | runtime support | |
netcdf | 4.7.0 | netcdf/4.7 | compiler/intel/19 compiler/intel/20 | library | runtime support | |
netcdf | 4.7.4 | netcdf/4.7 | compiler/gcc/10 compiler/gcc/9 compiler/gcc/11 | library | runtime support | |
netica-c | 5.04 | netica-c/5.04 | compiler/gcc/9 | library | mathematics | |
netlogo | 6.2.2 | netlogo/6.2 | None | application | Simulation | NetLogo is a multi-agent programmable modeling environment |
netsurfp | 1.0c | netsurfp/1.0 | None | application | computational biology | NetSurfP predicts the surface accessibility and secondary structure of amino acids in an amino acid sequence. The method also simultaneously predicts the reliability for each prediction, in the form of a Z-score. The Z-score is related to the surface prediction, and not the secondary structure. |
nextdenovo | 2.5.0 | nextdenovo/2.5 | None | application | Bioinformatics | String graph-based de novo assembler for long reads (CLR, HiFi and ONT) |
nextflow | 20.04.1 | nextflow/20.04 | None | application | computational pipeline | A DSL for data-driven computational pipelines http://nextflow.io |
nextflow | 21.04.0 | nextflow/21.04 | None | application | computational pipeline | A DSL for data-driven computational pipelines http://nextflow.io |
nextflow | 21.10.6 | nextflow/21.10 | None | application | computational pipeline | A DSL for data-driven computational pipelines http://nextflow.io |
nextflow | 22.10.6 | nextflow/22.10 | None | application | computational pipeline | A DSL for data-driven computational pipelines http://nextflow.io |
nextflow | 23.04.1 | nextflow/23.04 | None | application | computational pipeline | A DSL for data-driven computational pipelines http://nextflow.io |
nextflow | 23.10.1 | nextflow/23.10 | None | application | computational pipeline | A DSL for data-driven computational pipelines http://nextflow.io |
nextflow | 24.04.3 | nextflow/24.04 | None | application | computational pipeline | A DSL for data-driven computational pipelines http://nextflow.io |
nextpolish | 1.4.1 | nextpolish/1.4 | None | application | computational biology | Fast and accurately polish the genome generated by long reads |
nextstrain-cli | 1.16.2 | nextstrain-cli/1.16 | None | application | computational biology | Nextstrain: analysis and visualization of pathogen sequence data. |
nextstrain-cli | 3.0.3 | nextstrain-cli/3.0 | None | application | computational biology | Nextstrain: analysis and visualization of pathogen sequence data. |
nextstrain-cli | 3.2.5 | nextstrain-cli/3.2 | None | application | computational biology | Nextstrain: analysis and visualization of pathogen sequence data. |
nextstrain-cli | 4.2.0 | nextstrain-cli/4.2 | None | application | computational biology | Nextstrain: analysis and visualization of pathogen sequence data. |
ngmlr | 0.2.7 | ngmlr/0.2 | None | application | computational biology | ngmlr is a long-read mapper designed to align PacBio or Oxford Nanopore reads to a reference genome and optimized for structural variation detection |
ninja | 1.10.2 | ninja/1.10 | None | application | Utility | A small build system with a focus on speed |
ninja | 1.12.1 | ninja/1.12 | None | application | Utility | A small build system with a focus on speed |
nlopt | 2.7.1 | nlopt/py39/2.7 | None | application | algorithms | nonlinear optimization library |
nodejs | 16.6.1 | nodejs/16.6 | None | application | system | a platform for easily building fast, scalable network applications |
nofold | 1.0.1 | nofold/1.0 | None | application | computational biology | NoFold is an approach for characterizing and clustering RNA secondary structures without computational folding or alignment. |
nomad | 2.0.0 | nomad/2.0 | None | application | computational biology | NOMAD is an unsupervised and reference-free unifying framework to discover regulated sequence variation through statistical analysis of k-mer composition in both DNA and RNA sequence. |
nquire | 2018.04.05 | nquire/2018.04.05 | None | application | computational biology | A statistical framework for ploidy estimation using NGS short-read data. |
nucdiff | 2.0.2 | nucdiff/2.0 | None | application | computational biology | NucDiff locates and categorizes differences between two closely related nucleotide sequences. |
nvim | 0.9.5 | nvim/0.9 | None | application | utility | Ambitious Vim-fork focused on extensibility and agility |
nwchem | 7.0.2 | nwchem/7.0 | compiler/gcc/9:openmpi/4.1 | library | runtime support | |
nwchem | 7.2.2 | nwchem/7.2 | compiler/gcc/9:openmpi/4.1 | library | runtime support | |
oases | 0.2.09 | oases/0.2 | None | application | computational biology | Oases is de novo transcriptome assembler based on the Velvet genome assembler core. |
octave | 4.2 | octave/4.2 | None | application | engineering | GNU Octave is a high-level language, primarily intended for numerical computations. It provides a convenient command line interface for solving linear and nonlinear problems numerically, and for performing other numerical experiments using a language that is mostly compatible with Matlab. |
octave | 6.1 | octave/6.1 | None | application | engineering | GNU Octave is a high-level language, primarily intended for numerical computations. It provides a convenient command line interface for solving linear and nonlinear problems numerically, and for performing other numerical experiments using a language that is mostly compatible with Matlab. |
octave | 6.2 | octave/6.2 | None | application | engineering | GNU Octave is a high-level language, primarily intended for numerical computations. It provides a convenient command line interface for solving linear and nonlinear problems numerically, and for performing other numerical experiments using a language that is mostly compatible with Matlab. |
octave | 7.2 | octave/7.2 | None | application | engineering | GNU Octave is a high-level language, primarily intended for numerical computations. It provides a convenient command line interface for solving linear and nonlinear problems numerically, and for performing other numerical experiments using a language that is mostly compatible with Matlab. |
octopus | 13.0 | octopus/13.0 | compiler/intel/20:openmpi/4.1 | application | Applications | |
oma | 2.4.1 | oma/2.4 | None | application | genomics | OMA standalone is a standalone package that can infer orthologs using the OMA algorithm on custom genomes. |
oncodriveclustl | 1.1.3 | oncodriveclustl/1.1 | None | application | Biology | OncodriveCLUSTL is a clustering method to identify cancer drivers |
oncotator | 1.9.9.0 | oncotator/1.9 | None | application | computational biology | Oncotator is a tool for annotating human genomic point mutations and indels with data relevant to cancer researchers. |
openbabel | 3.1.1 | openbabel/py37/3.1 | None | application | chemistry | A chemical toolbox designed to speak the many languages of chemical data |
openbabel | 3.1.1 | openbabel/py38/3.1 | None | application | chemistry | A chemical toolbox designed to speak the many languages of chemical data |
openblas | 0.3.18 | openblas/0.3 | compiler/gcc/10 compiler/gcc/9 | library | tools | Numerical library, contains blas/lapack |
openbugs | 3.2 | openbugs/3.2 | None | application | statistics | BUGS is a software package for performing Bayesian inference Using Gibbs Sampling. |
opencl | 1.2 | opencl/1.2 | None | library | unknown | This runtime software package adds OpenCL CPU device support on systems with Intel Core and Intel Xeon processors. |
opencv | 2.4.11 | opencv/2.4 | None | library | unknown | Open Source Computer Vision Library |
opencv | 3.1.0 | opencv/3.1 | None | library | unknown | Open Source Computer Vision Library |
opencv | 3.4.1 | opencv/py27/3.4 | None | library | unknown | Open Source Computer Vision Library |
opencv | 3.4.1 | opencv/py36/3.4 | None | library | unknown | Open Source Computer Vision Library |
opencv | 4.2.0 | opencv/py27/4.2 | None | library | unknown | Open Source Computer Vision Library |
opencv | 4.2.0 | opencv/py37/4.2 | None | library | unknown | Open Source Computer Vision Library |
opencv | 4.2.0 | opencv/py38/4.2 | None | library | unknown | Open Source Computer Vision Library |
opencv | 4.5.5 | opencv/4.5 | compiler/gcc/11 | library | unknown | Open Source Computer Vision Library |
opencv | 4.8.1 | opencv/4.8 | compiler/gcc/11 | library | unknown | Open Source Computer Vision Library |
openfoam | 9 | openfoam/9.0 | compiler/gcc/11:openmpi/4.1 | library | runtime support | |
openjdk | 10 | openjdk/10 | None | application | system | OpenJDK (Java). |
openjdk | 11 | openjdk/11 | None | application | system | OpenJDK (Java). |
openjdk | 12 | openjdk/12 | None | application | system | OpenJDK (Java). |
openjdk | 13 | openjdk/13 | None | application | system | OpenJDK (Java). |
openjdk | 14 | openjdk/14 | None | application | system | OpenJDK (Java). |
openjdk | 15 | openjdk/15 | None | application | system | OpenJDK (Java). |
openjdk | 16 | openjdk/16 | None | application | system | OpenJDK (Java). |
openjdk | 17 | openjdk/17 | None | application | system | OpenJDK (Java). |
openjdk | 18 | openjdk/18 | None | application | system | OpenJDK (Java). |
openjdk | 19 | openjdk/9 | None | application | system | OpenJDK (Java). |
openjdk | 19 | openjdk/19 | None | application | system | OpenJDK (Java). |
openjdk | 20 | openjdk/20 | None | application | system | OpenJDK (Java). |
openjdk | 21 | openjdk/21 | None | application | system | OpenJDK (Java). |
openjdk | 22 | openjdk/22 | None | application | system | OpenJDK (Java). |
openjpeg | 2.3.1 | openjpeg/2.3 | compiler/pgi/20 | library | runtime support | |
openjpeg | 2.4 | openjpeg/2.4 | compiler/intel/20 compiler/pgi/20 compiler/gcc/10 compiler/intel/19 compiler/gcc/9 | library | runtime support | |
openmolcas | 23.06 | openmolcas/23.06 | compiler/intel/20:openmpi/4.1 | application | quantum chemistry software package | OpenMolcas is a quantum chemistry software package developed by scientists and intended to be used by scientists. It includes programs to apply many different electronic structure methods to chemical systems, but its key feature is the multiconfigurational approach, with methods like CASSCF and CASPT2. |
openmpi | 3.1 | openmpi/3.1 | compiler/nvhpc/21.9 | library | runtime support | |
openmpi | 4.0 | openmpi/4.0 | compiler/intel/19 compiler/intel/18 compiler/gcc/10 compiler/gcc/9 compiler/intel/16 compiler/intel/20 compiler/gcc/11 compiler/pgi/20 | library | runtime support | |
openmpi | 4.1 | openmpi/4.1 | compiler/intel/2021 compiler/intel/2024 compiler/gcc/10 compiler/pgi/20 compiler/intel/20 compiler/gcc/9 compiler/intel/18 compiler/gcc/11 compiler/intel/19 | library | runtime support | |
openmx | 3.9 | openmx/3.9 | compiler/intel/20:openmpi/4.1 compiler/intel/20:openmpi/4.0 | library | runtime support | |
openslide | 3.4.1 | openslide/3.4 | None | application | images | OpenSlide is a C library that provides a simple interface to read whole-slide images (also known as virtual slides). |
optuna | 2.8.0 | optuna/py37/2.8 | None | application | Mathematics | A hyperparameter optimization framework |
optuna | 2.8.0 | optuna/py38/2.8 | None | application | Mathematics | A hyperparameter optimization framework |
optuna | 2.8.0 | optuna/py39/2.8 | None | application | Mathematics | A hyperparameter optimization framework |
orca | 5.0.4 | orca/5.0 | compiler/gcc/11:openmpi/4.1 | application | quantum chemistry | ORCA is an ab initio, DFT, and semi-empirical SCF-MO package. |
orca | 6.0.0 | orca/6.0 | compiler/gcc/11:openmpi/4.1 | application | quantum chemistry | ORCA is an ab initio, DFT, and semi-empirical SCF-MO package. |
orthofinder | 1.1.8 | orthofinder/1.1 | None | application | computational biology | OrthoFinder is a fast, accurate and comprehensive analysis tool for comparative genomics. |
orthofinder | 2.2.6 | orthofinder/2.2 | None | application | computational biology | OrthoFinder is a fast, accurate and comprehensive analysis tool for comparative genomics. |
orthofinder | 2.5.5 | orthofinder/2.5 | None | application | computational biology | OrthoFinder is a fast, accurate and comprehensive analysis tool for comparative genomics. |
orthomcl | 2.0.9 | orthomcl/2.0 | None | application | Biology | Ortholog groups of protein sequences |
p7zip | 16.02 | p7zip/16.02 | None | application | System | p7zip is a quick port of 7z.exe and 7za.exe (command line version of 7zip, see www.7-zip.org ) for Unix. |
paml | 4.9 | paml/4.9 | None | application | Sequencing | Phylogenetic Analysis by Maximum Likelihood (PAML) |
pandaseq | 2.11 | pandaseq/2.11 | None | application | bioinformatics | PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the sequence, and reconstruct an overlapping sequence. |
panphlan | 1.3 | panphlan/1.3 | None | application | biology | PanPhlAn is a strain-level metagenomic profiling tool for identifying the gene composition and in-vivo transcriptional activity of individual strains in metagenomic samples. |
panphlan | 3.0 | panphlan/3.0 | None | application | biology | PanPhlAn is a strain-level metagenomic profiling tool for identifying the gene composition and in-vivo transcriptional activity of individual strains in metagenomic samples. |
parallel-fastq-dump | 0.6.5 | parallel-fastq-dump/0.6 | None | application | bioinformatics | parallel fastq-dump wrapper |
paraview | 5.10.1 | paraview/py37/5.10 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.10.1 | paraview/py38/5.10 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.10.1 | paraview/py39/5.10 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.11.1 | paraview/py39/5.11 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.11.1 | paraview/py310/5.11 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.11.1 | paraview/py311/5.11 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.9.1 | paraview/py37/5.9 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.9.1 | paraview/py38/5.9 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview | 5.9.1 | paraview/py39/5.9 | None | application | Utility | ParaView is an open-source, multi-platform data analysis and visualization application based on Visualization Toolkit (VTK). |
paraview-headless | 5.10 | paraview-headless/5.10 | compiler/gcc/11:openmpi/4.1 | application | Visualization | |
parmetis | 4.0.3 | parmetis/4.0 | compiler/pgi/20:openmpi/4.0 compiler/intel/19:openmpi/4.0 compiler/gcc/10:openmpi/4.0 compiler/intel/20:openmpi/4.0 compiler/gcc/9:openmpi/4.0 compiler/intel/20:openmpi/4.1 compiler/gcc/11:openmpi/4.1 | library | runtime support | |
parsinsert | 1.04 | parsinsert/1.04 | None | application | computational biology | ParsInsert efficiently produces both a phylogenetic tree and taxonomic classification for sequences for microbial community sequence analysis. This is a C++ implementation of the Parsimonious Insertion algorithm |
pasa | 2.3.3 | pasa/2.3 | None | application | computational biology | PASA |
pb-assembly | 0.0.8 | pb-assembly/0.0.8 | None | application | Genomics | Meta-package for Falcon/Unzip tool-suite (originally by Jason Chin) |
pbh5tools | 0.8.0 | pbh5tools/0.8 | None | application | computational biology | pbh5tools -- tools for manipulating HDF5 files produced by Pacific Biosciences. Specifically, this package provides functionality for manipulating and extracting data from "cmp.h5" and "bas.h5" files. |
pblat | 2.0 | pblat/2.0 | None | application | computational biology | |
peakranger | 1.18 | peakranger/1.18 | None | application | computational biology | PeakRanger is a multi-purporse software suite for analyzing next-generation sequencing (NGS) data. |
peakzilla | 1.0 | peakzilla/1.0 | None | application | computational biology | Peakzilla identifies sites of enrichment and transcription factor binding sites from transcription factor ChIP-seq and ChIP-exo experiments at hight accuracy and resolution. |
pegasus-wms | 5.0 | pegasus-wms/5.0 | None | application | workflow management system | Pegasus Workflow Management System |
pepr | 1.1.18 | pepr/1.1 | None | application | computational biology | Peak-calling and Prioritization pipeline for replicated ChIP-Seq data. |
perl | 5.22 | perl/5.22 | None | application | perl | The Perl Programming Language |
perl | 5.26.2 | perl/5.26 | None | application | perl | The Perl Programming Language |
perl-mongodb | 1.2.2 | perl-mongodb/1.2 | None | application | Utility | This is the official Perl driver for MongoDB. |
perl-pcap | 3.5.2 | perl-pcap/3.5 | None | application | computational biology | NGS reference implementations and helper code for the IGCG/TCGA Pan-Cancer Analysis Project |
petsc | 3.15 | petsc/3.15 | compiler/intel/20:openmpi/4.1 compiler/intel/20:openmpi/4.0 compiler/gcc/10:openmpi/4.0 | library | runtime support | |
phast | 1.5 | phast/1.5 | None | application | bioinformatics | PHAST is a freely available software package for comparative and evolutionary genomics. |
phdf5 | 1.12.0 | phdf5/1.12 | compiler/intel/20:openmpi/4.1 compiler/gcc/10:openmpi/4.1 compiler/intel/19:openmpi/4.0 compiler/gcc/10:openmpi/4.0 compiler/gcc/9:openmpi/4.1 compiler/gcc/9:openmpi/4.0 compiler/intel/20:openmpi/4.0 compiler/intel/19:openmpi/4.1 | library | runtime support | |
phenix | 1.18.2 | phenix/1.18 | compiler/gcc/9 | library | runtime support | |
phenix | 1.19.2 | phenix/1.19 | compiler/gcc/9 | library | runtime support | |
phist | 1.0.0 | phist/1.0 | None | application | computational biology | Phage-Host Interaction Search Tool. |
phobius | 1.01 | phobius/1.01 | None | application | computational biology | Phobius is a combined transmembrane topology and signal peptide predictor. |
phono3py | 1.18.1+3 | phono3py/py27/1.18 | None | application | Simulation | A simulation package of phonon-phonon interaction related properties |
phono3py | 1.18.1+3 | phono3py/py36/1.18 | None | application | Simulation | A simulation package of phonon-phonon interaction related properties |
phono3py | 1.18.1+3 | phono3py/py37/1.18 | None | application | Simulation | A simulation package of phonon-phonon interaction related properties |
phono3py | 2.1.0 | phono3py/py38/2.1 | None | application | Simulation | A simulation package of phonon-phonon interaction related properties |
phono3py | 2.1.0 | phono3py/py39/2.1 | None | application | Simulation | A simulation package of phonon-phonon interaction related properties |
phonopy | 1.11.12 | phonopy/1.11 | None | library | runtime support | |
phonopy | 2.11.0 | phonopy/py37/2.11 | None | library | runtime support | |
phonopy | 2.11.0 | phonopy/py39/2.11 | None | library | runtime support | |
phylip | 3.697 | phylip/3.6 | None | library | runtime support | |
phyloflash | 3.4 | phyloflash/3.4 | None | application | Phylogeny | phyloFlash is a pipeline to rapidly reconstruct the SSU rRNAs and explore phylogenetic composition of an illumina (meta)genomic dataset. |
phylogenetics | 0.5.0 | phylogenetics/0.5 | None | application | computational biology | Python API for managing a phylogenetics projects. |
phylophlan | 1.0 | phylophlan/1.0 | None | application | computational biology | Precise phylogenetic analysis of microbial isolates and genomes from metagenomes |
phylophlan | 3.0.2 | phylophlan/3.0 | None | application | computational biology | Precise phylogenetic analysis of microbial isolates and genomes from metagenomes |
phylosnp | 1.0 | phylosnp/1.0 | None | application | computational biology | PhyloSNP is designed to take SNP data files (.csv and .vcf) and generate phylogenetic trees from the provided data. |
phyluce | 1.6.8 | phyluce/1.6 | None | application | Genome reduction | Software for UCE (and general) phylogenomics, and it is a software package that was initially developed for analyzing data collected from ultraconserved elements in organismal genomes. |
phyml | 3.3.20180621 | phyml/3.3 | None | application | Biology | Phylogenetic estimation using (Maximum) Likelihood |
picard | 1.139 | picard/1.1 | None | application | computational biology | A set of Java command line tools for manipulating high-throughput sequencing data (HTS) data and formats. |
picard | 2.13 | picard/2.13 | None | application | computational biology | A set of Java command line tools for manipulating high-throughput sequencing data (HTS) data and formats. |
picard | 2.18.4 | picard/2.18 | None | application | computational biology | A set of Java command line tools for manipulating high-throughput sequencing data (HTS) data and formats. |
picard | 2.22.2 | picard/2.22 | None | application | computational biology | A set of Java command line tools for manipulating high-throughput sequencing data (HTS) data and formats. |
picard | 2.9.0 | picard/2.9 | None | application | computational biology | A set of Java command line tools for manipulating high-throughput sequencing data (HTS) data and formats. |
picard | 3.0.0 | picard/3.0 | None | application | computational biology | A set of Java command line tools for manipulating high-throughput sequencing data (HTS) data and formats. |
picrust | 1.1.0 | picrust/1.1 | None | application | metagenomic | The PICRUSt project aims to support prediction of the unobserved character states in a community of organisms from phylogenetic information about the organisms in that community. |
picrust2 | 2.2.0_b | picrust2/2.2 | None | application | Pipeline | PICRUSt: Phylogenetic Investigation of Communities by Reconstruction of Unobserved States |
picrust2 | 2.4.1 | picrust2/2.4 | None | application | Pipeline | PICRUSt: Phylogenetic Investigation of Communities by Reconstruction of Unobserved States |
picrust2 | 2.5.2 | picrust2/2.5 | None | application | Pipeline | PICRUSt: Phylogenetic Investigation of Communities by Reconstruction of Unobserved States |
pilon | 1.23 | pilon/1.23 | None | application | bioinformatics | Pilon is an automated genome assembly improvement and variant detection tool. |
pilon | 1.24 | pilon/1.24 | None | application | bioinformatics | Pilon is an automated genome assembly improvement and variant detection tool. |
pindel | 0.2.5b9 | pindel/0.2 | None | application | computational biology | |
pirs | 2.0.2 | pirs/2.0 | None | application | computational biology | |
plasmidfinder | 2.0.1 | plasmidfinder/2.0 | None | application | computational biology | PlasmidFinder allows identification of plasmids in total or partial sequenced isolates of bacteria. |
plasmidfinder | 2.1 | plasmidfinder/2.1 | None | application | computational biology | PlasmidFinder allows identification of plasmids in total or partial sequenced isolates of bacteria. |
plink | 1.90b4 | plink/1.90 | None | application | computational biology | PLINK is a free, open-source whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner. |
plink2 | 2.0a1 | plink2/2.0a1 | None | application | computational biology | This is a comprehensive update to Shaun Purcell's PLINK command-line program, developed by Christopher Chang with support from the NIH-NIDDK's Laboratory of Biological Modeling, the Purcell Lab at Mount Sinai School of Medicine, and others. |
plinkseq | 0.10 | plinkseq/0.10 | None | application | computational biology | PLINK/SEQ is an open-source C/C++ library for working with human genetic variation data. |
plumed | 2.8.0 | plumed/2.8 | compiler/gcc/10:openmpi/4.1 | application | molecular dynamics | The community-developed PLUgin for MolEcular Dynamics. |
plumed | 2.8.1 | plumed/2.8 | compiler/gcc/11:openmpi/4.1 compiler/intel/20:openmpi/4.1 | application | molecular dynamics | The community-developed PLUgin for MolEcular Dynamics. |
plumed | 2.9.0 | plumed/2.9 | compiler/intel/20:openmpi/4.1 compiler/gcc/11:openmpi/4.1 | application | molecular dynamics | The community-developed PLUgin for MolEcular Dynamics. |
pmlst | 2.0.3 | pmlst/2.0 | None | application | Bioinformatics | Plasmid Multi-Locus Sequence Typing |
pomoxis | 0.1.7 | pomoxis/0.1 | None | application | computational biology | Assembly, consensensus, and analysis tools by ONT research |
pomoxis | 0.3.13 | pomoxis/0.3 | None | application | computational biology | Assembly, consensensus, and analysis tools by ONT research |
poplddecay | 3.42 | poplddecay/3.42 | None | application | computational biology | Fast and effective tool for linkage disequilibrium decay analysis. |
popoolation2 | 1.201 | popoolation2/1.201 | None | application | Genomics | PoPoolation2 allows to compare allele frequencies for SNPs between two or more populations and to identify significant differences. |
poppunk | 1.1.6 | poppunk/1.1 | None | application | computational biology | PopPUNK (POPulation Partitioning Using Nucleotide Kmers) |
postgresql | 15.2 | postgresql/15.2 | None | application | database | PostgreSQL is a powerful, open source object-relational database system. |
povray | 3.7.0.8 | povray/3.7 | None | application | CGI | The Persistence of Vision Raytracer. |
pplacer | 1.1 | pplacer/1.1 | None | application | computational biology | Pplacer places query sequences on a fixed reference phylogenetic tree to maximize phylogenetic likelihood or posterior probability according to a reference alignment. |
prank | v.170427 | prank/170427 | None | application | bioinformatics | PRANK is a probabilistic multiple alignment program for DNA, codon and amino-acid sequences. |
primer3 | 2.3.7 | primer3/2.3 | None | application | computational biology | Primer3 picks primers for PCR reactions |
prinseq-lite | 0.20.4 | prinseq-lite/0.20 | None | application | computational biology | PRINSEQ can be used to filter, reformat, or trim your genomic and metagenomic sequence data |
prodigal | 2.6.3 | prodigal/2.6 | None | application | computational biology | Prodigal (Prokaryotic Dynamic Programming Genefinding Algorithm) is a microbial (bacterial and archaeal) gene finding program developed at Oak Ridge National Laboratory and the University of Tennessee. |
prodigal | 2.60 | prodigal/2.60 | None | application | computational biology | Prodigal (Prokaryotic Dynamic Programming Genefinding Algorithm) is a microbial (bacterial and archaeal) gene finding program developed at Oak Ridge National Laboratory and the University of Tennessee. |
prohlatype | 0.9.0 | prohlatype/0.9 | None | application | Computational Biology | This project provides a set of tools to calculate the full posterior distribution of HLA types given read data. |
proj | 7.1.1 | proj/7.1 | compiler/intel/20 compiler/pgi/20 compiler/intel/19 compiler/gcc/9 compiler/gcc/10 | library | runtime support | |
prokka | 1.12 | prokka/1.12 | None | application | bioinformatics | Prokka is a software tool for the rapid annotation of prokaryotic genomes. |
prokka | 1.13.7 | prokka/1.13 | None | application | bioinformatics | Prokka is a software tool for the rapid annotation of prokaryotic genomes. |
prokka | 1.14.6 | prokka/1.14 | None | application | bioinformatics | Prokka is a software tool for the rapid annotation of prokaryotic genomes. |
proteowizard | 3_0_9992 | proteowizard/3.0 | None | application | computational biology | ProteoWizard provides a modular and extensible set of open-source, cross-platform tools and libraries. |
provean | 1.1.5 | provean/1.1 | None | application | computational biology | PROVEAN (Protein Variation Effect Analyzer) is a software tool which predicts whether an amino acid substitution or indel has an impact on the biological function of a protein. |
psi4 | 1.9.1 | psi4/py310/1.9 | None | application | quantum chemistry | Open-Source Quantum Chemistry - an electronic structure package in C++ driven by Python |
psi4 | 1.9.1 | psi4/py311/1.9 | None | application | quantum chemistry | Open-Source Quantum Chemistry - an electronic structure package in C++ driven by Python |
pullseq | 1.0 | pullseq/1.0 | None | application | computational biology | pullseq - Software to extract sequence from a fasta or fastq. Also filter sequences by a minimum length or maximum length. |
purge_dups | 1.2.6 | purge_dups/1.2 | None | application | Biology | Purge_dups is a package used to purge haplotigs and overlaps in an assembly based on read depth |
pwtools | 1.2.2 | pwtools/py37/1.2 | None | application | python | pwtools is a Python package for pre- and postprocessing of atomistic calculations, mostly targeted to Quantum Espresso, CPMD, CP2K and LAMMPS. |
pwtools | 1.2.2 | pwtools/py39/1.2 | None | application | python | pwtools is a Python package for pre- and postprocessing of atomistic calculations, mostly targeted to Quantum Espresso, CPMD, CP2K and LAMMPS. |
pyani | 0.2.11 | pyani/py39/0.2 | None | application | computational biology | pyani provides a package and script for calculation of genome-scale average nucleotide identity. |
pyclone | 0.13 | pyclone/0.13 | None | application | computational biology | PyClone is statistical model and software tool designed to infer the prevalence of point mutations in heterogeneous cancer samples. |
pydeface | 2.0.2 | pydeface/2.0 | None | application | neuroimaging | A tool to remove facial structure from MRI images. |
pyfasta | 0.5 | pyfasta/0.5 | None | application | computational biology | Pyfasta - fast, memory-efficient, pythonic (and command-line) access to fasta sequence files. |
pygenometracks | 2.0 | pygenometracks/2.0 | None | application | bioinformatics | Standalone program and library to plot beautiful genome browser tracks. |
pyicoteo | 2.0.7 | pyicoteo/2.0 | None | application | Biology | Analysis and manipulation of mapped reads coming from High Throughput Sequencing tool and library. |
pymagic | 0.1 | pymagic/0.1 | None | application | computational biology | MAGIC: A diffusion-based imputation method reveals gene-gene interactions in single-cell RNA-sequencing data. |
pymatgen | 2023.6.28 | pymatgen/py39/2023.6.28 | None | application | materials analysis | Python Materials Genomics is an analysis code for materials science. |
pymatgen | 2023.6.28 | pymatgen/py310/2023.6.28 | None | application | materials analysis | Python Materials Genomics is an analysis code for materials science. |
pymatgen | 2023.6.28 | pymatgen/py311/2023.6.28 | None | application | materials analysis | Python Materials Genomics is an analysis code for materials science. |
pymeteo | 0.5 | pymeteo/0.5 | None | application | geoscience | General meteorological routines, skew-T/log-p plotting and working with CM1 model data. |
pymlst | 0.0.2020.06.19 | pymlst/2020.06.19 | None | application | computational biology | python Mlst Local Search Tool |
pymol-open-source | 2.4.0 | pymol-open-source/py37/2.4 | None | application | Molecular Dynamics | A user-sponsored molecular visualization system |
pymol-open-source | 2.4.0 | pymol-open-source/py38/2.4 | None | application | Molecular Dynamics | A user-sponsored molecular visualization system |
pymol-open-source | 2.4.0 | pymol-open-source/py39/2.4 | None | application | Molecular Dynamics | A user-sponsored molecular visualization system |
pymol-open-source | 2.5.0 | pymol-open-source/py39/2.5 | None | application | Molecular Dynamics | A user-sponsored molecular visualization system |
pymol-open-source | 2.5.0 | pymol-open-source/py310/2.5 | None | application | Molecular Dynamics | A user-sponsored molecular visualization system |
pymol-open-source | 2.5.0 | pymol-open-source/py311/2.5 | None | application | Molecular Dynamics | A user-sponsored molecular visualization system |
pymongo | 3.0.3 | pymongo/3.0 | None | application | Utility | PyMongo is a Python distribution containing tools for working with MongoDB, and is the recommended way to work with MongoDB from Python. |
pymongo | 3.3.0 | pymongo/3.3 | None | application | Utility | PyMongo is a Python distribution containing tools for working with MongoDB, and is the recommended way to work with MongoDB from Python. |
pymongo | 3.7.2 | pymongo/3.7 | None | application | Utility | PyMongo is a Python distribution containing tools for working with MongoDB, and is the recommended way to work with MongoDB from Python. |
pysam | 0.16.0.1 | pysam/py37/0.16 | None | application | bioinformatics | Pysam is a python module for reading and manipulating Samfiles. |
pysam | 0.16.0.1 | pysam/py38/0.16 | None | application | bioinformatics | Pysam is a python module for reading and manipulating Samfiles. |
pyseer | 1.2.0 | pyseer/1.2 | None | application | computational biology | Sequence Elements Enrichment Analysis (SEER), python implementation |
pyseer | 1.3.4 | pyseer/1.3 | None | application | computational biology | Sequence Elements Enrichment Analysis (SEER), python implementation |
python | 2.7 | python/2.7 | None | application | system | |
python | 3.10 | python/3.10 | None | application | system | |
python | 3.11 | python/3.11 | None | application | system | |
python | 3.3 | python/3.3 | None | application | system | |
python | 3.4 | python/3.4 | None | application | system | |
python | 3.5 | python/3.5 | None | application | system | |
python | 3.6 | python/3.6 | None | application | system | |
python | 3.7 | python/3.7 | None | application | system | |
python | 3.8 | python/3.8 | None | application | system | |
python | 3.9 | python/3.9 | None | application | system | |
python-openstackclient | 2.1.0 | python-openstackclient/2.1 | None | application | Utility | Client for OpenStack services |
python-openstackclient | 6.0.0 | python-openstackclient/6.0 | None | application | Utility | Client for OpenStack services |
pytorch | 0.4.1 | pytorch/py27/0.4 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 0.4.1 | pytorch/py35/0.4 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 0.4.1 | pytorch/py36/0.4 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.10.0 | pytorch/py38/1.10 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.10.0 | pytorch/py39/1.10 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.12.1 | pytorch/py38/1.12 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.12.1 | pytorch/py39/1.12 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.13.0 | pytorch/py39/1.13 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.13.0 | pytorch/py310/1.13 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.2.0 | pytorch/py27/1.2 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.2.0 | pytorch/py36/1.2 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.2.0 | pytorch/py37/1.2 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.5.1 | pytorch/py37/1.5 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.6.0 | pytorch/py37/1.6 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.7.1 | pytorch/py37/1.7 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.7.1 | pytorch/py38/1.7 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.8.0 | pytorch/py37/1.8 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.8.0 | pytorch/py38/1.8 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 1.8.0 | pytorch/py39/1.8 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 2.0.0 | pytorch/py310/2.0 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 2.0.0 | pytorch/py311/2.0 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 2.3.1 | pytorch/py39/2.3 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch | 2.3.1 | pytorch/py311/2.3 | None | application | deep learning | PyTorch is an optimized tensor library for deep learning using GPUs and CPUs. |
pytorch-gpu | 1.10.0 | pytorch-gpu/py38/1.10 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 1.10.0 | pytorch-gpu/py39/1.10 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 1.12.1 | pytorch-gpu/py38/1.12 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 1.12.1 | pytorch-gpu/py39/1.12 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 1.13.0 | pytorch-gpu/py39/1.13 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 1.13.0 | pytorch-gpu/py310/1.13 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 1.8.0 | pytorch-gpu/py38/1.8 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 1.9.0 | pytorch-gpu/py38/1.9 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 2.0.0 | pytorch-gpu/py310/2.0 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 2.0.0 | pytorch-gpu/py311/2.0 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 2.3.1 | pytorch-gpu/py39/2.3 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
pytorch-gpu | 2.3.1 | pytorch-gpu/py311/2.3 | None | application | deep learning | Tensors and Dynamic neural networks in Python with strong GPU acceleration |
qctool | 1.4 | qctool/1.4 | None | application | computational biology | QCTOOL is a command-line utility program for basic quality control of gwas datasets. |
qgis | 3.18.3 | qgis/3.18 | None | application | geographic information system | A free and open source Geographic Information System (GIS). |
qgis | 3.30.2 | qgis/3.30 | None | application | geographic information system | A free and open source Geographic Information System (GIS). |
qgrs-cpp | 2017.08.25 | qgrs-cpp/2017.08.25 | None | application | computational biology | C++ implementation of QGRS mapping. |
qiime | 1.9.1 | qiime/1.9 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime | 2017.9 | qiime/2.0 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2017.9 | qiime2/2017.9 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2018.2 | qiime2/2018.2 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2018.4 | qiime2/2018.4 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2019.1 | qiime2/2019.1 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2019.10 | qiime2/2019.10 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2020.2.0 | qiime2/2020.2 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2021.11.0 | qiime2/2021.11 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2021.2 | qiime2/2021.2 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2021.4.0 | qiime2/2021.4 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2022.2.0 | qiime2/2022.2 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qiime2 | 2024.5.0 | qiime2/2024.5 | None | application | computational biology | QIIME 2 is a powerful, extensible, and decentralized microbiome analysis package with a focus on data and analysis transparency. |
qmpy | 1.4.0 | qmpy/py36/1.4 | None | application | Physics | A suite of computational materials science tools. |
qmpy | 1.4.0 | qmpy/py37/1.4 | None | application | Physics | A suite of computational materials science tools. |
qmpy | 1.4.0 | qmpy/py38/1.4 | None | application | Physics | A suite of computational materials science tools. |
quake | 0.3.5 | quake/0.3 | None | application | computational biology | Quake is a package to correct substitution sequencing errors in experiments with deep coverage. |
qualimap | 2.3 | qualimap/2.3 | None | application | sequencing alignment | Quality control of alignment sequencing data and its derivatives like feature counts |
quasr | 6.09 | quasr/6.09 | None | application | computational biology | QUASR is lightweight pipeline for processing and analysis of high-throughput sequencing data. |
quast | 4.1 | quast/4.1 | None | application | computational biology | QUAST evaluates genome assemblies by computing various metrics. |
quast | 4.4 | quast/4.4 | None | application | computational biology | QUAST evaluates genome assemblies by computing various metrics. |
quast | 4.5 | quast/4.5 | None | application | computational biology | QUAST evaluates genome assemblies by computing various metrics. |
quast | 5.0 | quast/5.0 | None | application | computational biology | QUAST evaluates genome assemblies by computing various metrics. |
r-asreml | 4.1 | r-asreml/r36/4.1 | None | application | data analysis | ASReml-R is a statistical package that fits linear mixed models using Residual Maximum Likelihood (REML) in the R environment. |
r-asreml | 4.1 | r-asreml/r40/4.1 | None | application | data analysis | ASReml-R is a statistical package that fits linear mixed models using Residual Maximum Likelihood (REML) in the R environment. |
r-asreml | 4.2 | r-asreml/r43/4.2 | None | application | data analysis | ASReml-R is a statistical package that fits linear mixed models using Residual Maximum Likelihood (REML) in the R environment. |
r-fastbaps | 1.0.1 | r-fastbaps/r36/1.0 | None | application | computational biology | A fast approximation to a Dirichlet Process Mixture model (DPM) for clustering genetic data |
r-fastbaps | 1.0.6 | r-fastbaps/r41/1.0 | None | application | computational biology | A fast approximation to a Dirichlet Process Mixture model (DPM) for clustering genetic data |
r-genometricorr | 1.1.17 | r-genometricorr/r33/1.1 | None | application | Genomics | Genometric Correlation (GenometriCorr) is an R package for spatial correlation of genome-wide interval datasets. |
r-ggfortify | 0.4.1 | r-ggfortify/r33/0.4 | None | application | r | ggfortify is a package of unified plotting tools for statistics commonly used, such as GLM, time series, PCA families, clustering and survival analysis. |
r-hmisc | 4.6_0 | r-hmisc/4.6 | None | application | statistics | Contains many functions useful for data analysis, high-level graphics, utility operations, functions for computing sample size and power, importing and annotating datasets, imputing missing values, advanced table making, variable clustering, character string manipulation, conversion of R objects to LaTeX and html code, and recoding variables. |
r-inla | 20.03.17 | r-inla/r36/20.03.17 | None | application | Mathematics | Full Bayesian Analysis of Latent Gaussian Models using Integrated Nested Laplace Approximations |
r-keras | 2.2.4.1 | r-keras/r35/2.2 | None | application | machine learning | Interface to 'Keras' <https://keras.io>, a high-level neural networks 'API'. |
r-markdown | 0.8 | r-markdown/r34/0.8 | None | application | R | Markdown is a plain-text formatting syntax that can be converted to XHTML or other formats. |
r-matlib | 0.9.2 | r-matlib/r36/0.9 | None | application | R | A collection of matrix functions for teaching and learning matrix linear algebra as used in multivariate statistical methods. |
r-regresshaplo | 1.0 | r-regresshaplo/r34/1.0 | None | application | biology | This package reconstructs haplotypes from a BAM file using a penalized regression approach. |
r-rhierbaps | 1.1.2 | r-rhierbaps/r35/1.1 | None | application | computational biology | rhierbaps is R implementation of hierBAPS. |
r-rrblup | 4.6.1 | r-rrblup/r41/4.6 | None | application | genomics | Software for genomic prediction with the RR-BLUP mixed model. |
r-scimpute | 0.0.5 | r-scimpute/0.0.5 | None | application | biology | scImpute is accurate and robust imputation of single-cell RNA sequencing data. |
r-scimpute | 0.0.6 | r-scimpute/r34/0.0.6 | None | application | biology | scImpute is accurate and robust imputation of single-cell RNA sequencing data. |
r-seqminer | 6.0 | r-seqminer/r34/6.0 | None | application | biology | SEQMINER is for sequencing variant annotation, data integration and query in R. |
r-seurat | 4.1.0 | r-seurat/r41/4.1 | None | application | computational biology | A toolkit for quality control, analysis, and exploration of single cell RNA sequencing data. |
r-vcfr | 1.5.0 | r-vcfr/r34/1.5 | None | application | biology | A package to manipulate and visualize VCF data in R. |
racon | 1.5.0 | racon/1.5 | None | application | bioinformatics | Ultrafast consensus module for raw de novo genome assembly of long uncorrected reads. |
rarefactionanalyzer | 2018.09.06 | rarefactionanalyzer/2018.09.06 | None | application | computational biology | Rarefaction analyzer is a simple program that can be used to perform rarefaction analysis. |
raxml | 8.2.12 | raxml/8.2 | None | application | Biology | Phylogenetics - Randomized Axelerated Maximum Likelihood. |
raxml-ng | 1.0.3 | raxml-ng/1.0 | compiler/gcc/10:openmpi/4.1 | application | Genetics | RAxML Next Generation: faster, easier-to-use and more flexible |
raxml-ng | 1.1.0 | raxml-ng/1.1 | compiler/gcc/10:openmpi/4.1 | application | Genetics | RAxML Next Generation: faster, easier-to-use and more flexible |
raxml-ng | 1.2.0 | raxml-ng/1.2 | compiler/gcc/10:openmpi/4.1 | application | Genetics | RAxML Next Generation: faster, easier-to-use and more flexible |
ray | 2.3.1 | ray/2.3 | None | application | computational biology | Ray is a parallel software that computes de novo genome assemblies with next-generation sequencing data. |
rclone | 1.44 | rclone/1.44 | None | application | Storage | Rclone ("rsync for cloud storage") is a command line program to sync files and directories to and from different cloud storage providers. |
rclone | 1.50.2 | rclone/1.50 | None | application | Storage | Rclone ("rsync for cloud storage") is a command line program to sync files and directories to and from different cloud storage providers. |
rclone | 1.51.0 | rclone/1.51 | None | application | Storage | Rclone ("rsync for cloud storage") is a command line program to sync files and directories to and from different cloud storage providers. |
rclone | 1.59.2 | rclone/1.59 | None | application | Storage | Rclone ("rsync for cloud storage") is a command line program to sync files and directories to and from different cloud storage providers. |
rclone | 1.64.2 | rclone/1.64 | None | application | Storage | Rclone ("rsync for cloud storage") is a command line program to sync files and directories to and from different cloud storage providers. |
read2tree | 0.1.5 | read2tree/py39/0.1 | None | application | computational biology | Building phylogenetic trees directly from sequencing reads |
read2tree | 0.1.5 | read2tree/py310/0.1 | None | application | computational biology | Building phylogenetic trees directly from sequencing reads |
readosm | 1.1 | readosm/1.1 | compiler/gcc/9 | unknown | unknown | |
readosm | 1.1.0a | readosm/1.1 | compiler/gcc/10 compiler/intel/19 compiler/intel/20 | unknown | unknown | |
reago | 1.1 | reago/1.1 | None | application | bioinformatics | Reconstructing 16S rRNA genes in metagenomic data. |
red | 2015.05.22 | red/2015.05.22 | None | application | Genomics | Red (RepeatsDetector): an intelligent, rapid, accurate tool for detecting repeats de-novo on the genomic scale. |
regtools | 0.5.0 | regtools/0.5 | None | application | bioinformatics | Tools that integrate DNA-seq and RNA-seq data to help interpret mutations in a regulatory and splicing context. |
relion | 4.0.0 | relion/4.0 | compiler/intel/20:openmpi/4.1 | application | Physics | |
relion-gpu | 4.0.0 | relion-gpu/4.0 | compiler/gcc/11:openmpi/4.1 | application | Physics | |
repeatmasker | 4.0 | repeatmasker/4.0 | None | application | computational biology | RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences. |
repenrich | 1.2 | repenrich/1.2 | None | application | computational biology | RepEnrich is a method to estimate repetitive element enrichment using high-throughput sequencing data. |
resfinder | 4.1.11 | resfinder/4.1 | None | application | unknown | ResFinder identifies acquired antimicrobial resistance genes in total or partial sequenced isolates of bacteria. |
resistomeanalyzer | 2018.09.06 | resistomeanalyzer/2018.09.06 | None | application | computational biology | Resistome Analyzer is a simple tool for analyzing the resistome of large metagenomic datasets. |
retroseq | 1.5 | retroseq/1.5 | None | application | bioinformatics | RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference transposable elements. |
revbayes | 1.2.2 | revbayes/1.2 | compiler/gcc/11:openmpi/4.1 | application | Bioinformatics | Bayesian Phylogenetic Inference Using Graphical Models and an Interactive Model-Specification Language. |
revtrans | 1.4 | revtrans/1.4 | None | application | computational biology | RevTrans - performs a reverse translation of a peptide alignment. |
rgi | 5.1.0 | rgi/5.1 | None | application | computational biology | Resistance gene identifier. |
rgi | 5.2.1 | rgi/5.2 | None | application | computational biology | Resistance gene identifier. |
rgi | 6.0.2 | rgi/6.0 | None | application | computational biology | Resistance gene identifier. |
rgt | 0.11.4 | rgt/0.11 | None | application | computational biology | Toolkit to perform regulatory genomics data analysis |
ripgrep | 13.0.0 | ripgrep/13.0 | None | application | Utility | ripgrep recursively searches directories for a regex pattern |
ripser | 1.0.1 | ripser/1.0 | None | application | Bioinformatics | Ripser: efficient computation of Vietoris–Rips persistence barcodes. |
rmats | 4.1.2 | rmats/4.1 | None | application | computational biology | MATS is a computational tool to detect differential alternative splicing events from RNA-Seq data. |
rmats | 4.3.0 | rmats/4.3 | None | application | computational biology | MATS is a computational tool to detect differential alternative splicing events from RNA-Seq data. |
rnaclust | 1.3 | rnaclust/1.3 | None | application | computational biology | A tool for clustering of RNAs based on their secondary structures using LocARNA |
rnahybrid | 2.1.2 | rnahybrid/2.1 | None | application | computational biology | RNAhybrid is a tool for finding the minimum free energy hybridization of a long and a short RNA. |
rnammer | 1.2 | rnammer/1.2 | None | application | computational biology | RNAmmer predicts 5s/8s, 16s/18s, and 23s/28s ribosomal RNA in full genome sequences. |
rnaquast | 1.5.1 | rnaquast/1.5 | None | application | Biology | rnaQUAST is a tool for evaluating RNA-Seq assemblies using reference genome and gene database. In addition, rnaQUAST is also capable of estimating gene database coverage by raw reads and de novo quality assessment using third-party software. |
rnasnp | 1.2 | rnasnp/1.2 | None | application | computational biology | Efficient detection of local RNA secondary structure changes induced by SNPs. |
rnastructure | 6.1 | rnastructure/6.1 | None | application | Bioinformatics | RNAstructure is a complete package for RNA and DNA secondary structure prediction and analysis. It includes algorithms for secondary structure prediction, including facility to predict base pairing probabilities. It also can be used to predict bimolecular structures and can predict the equilibrium binding affinity of an oligonucleotide to a structured RNA target. This is useful for siRNA design. It can also predict secondary structures common to two, unaligned sequences, which is much more accurate than single sequence secondary structure prediction. Finally, RNAstructure can take a number of different types of experiment mapping data to constrain or restrain structure prediction. These include chemical mapping, enzymatic mapping, NMR, and SHAPE data. |
roary | 3.12.0 | roary/3.12 | None | application | computational biology | Rapid large-scale prokaryote pan genome analysis |
roary | 3.13.0 | roary/3.13 | None | application | computational biology | Rapid large-scale prokaryote pan genome analysis |
rosetta | 3.12 | rosetta/3.12 | compiler/gcc/9:openmpi/4.1 | application | computational biology | The Rosetta software suite includes algorithms for computational modeling and analysis of protein structures. It has enabled notable scientific advances in computational biology, including de novo protein design, enzyme design, ligand docking, and structure prediction of biological macromolecules and macromolecular complexes. |
rosetta | 3.13 | rosetta/3.13 | compiler/gcc/9:openmpi/4.1 | application | computational biology | The Rosetta software suite includes algorithms for computational modeling and analysis of protein structures. It has enabled notable scientific advances in computational biology, including de novo protein design, enzyme design, ligand docking, and structure prediction of biological macromolecules and macromolecular complexes. |
rosettafold | 1.0.0 | rosettafold/1.0 | None | application | bioinformatics | RoseTTAFold - Accurate prediction of protein structures and interactions using a 3-track network. |
rosettafold2na | 0.2 | rosettafold2na/0.2 | None | application | computational biology | RoseTTAFold2 protein/nucleic acid complex prediction. |
rsem | 1.2 | rsem/1.2 | None | application | computational biology | RSEM is a software package for estimating gene and isoform expression levels from RNA-Seq data. |
rsem | 1.3 | rsem/1.3 | None | application | computational biology | RSEM is a software package for estimating gene and isoform expression levels from RNA-Seq data. |
rstudio | 2023.12 | rstudio/2023.12 | None | library | runtime support | RStudio is an integrated development environment (IDE) for R and Python. |
rsync | 3.1.3 | rsync/3.1 | None | application | System | Tool for fast incremental file transfer |
rsync | 3.2.3 | rsync/3.2 | None | application | System | Tool for fast incremental file transfer |
ruby | 2.1 | ruby/2.1 | None | application | system | |
rucs | 1.0.2 | rucs/1.0 | None | application | computational biology | RUCS is a bioinformatics tool developed to ease the task of designing new primers. |
rust | 1.41.0 | rust/1.41 | None | application | System | Rust is a systems programming language that runs blazingly fast, prevents segfaults, and guarantees thread safety. This package provides the compiler (rustc) and the documentation utilities rustdoc. |
saga-gis | 2.3 | saga-gis/py27/2.3 | None | application | Geoscience | SAGA - System for Automated Geoscience Analysis. |
saga-gis | 8.3.1 | saga-gis/py37/8.3 | None | application | Geoscience | SAGA - System for Automated Geoscience Analysis. |
saga-gis | 8.3.1 | saga-gis/py38/8.3 | None | application | Geoscience | SAGA - System for Automated Geoscience Analysis. |
saga-gis | 8.3.1 | saga-gis/py39/8.3 | None | application | Geoscience | SAGA - System for Automated Geoscience Analysis. |
sage | 6.3 | sage/6.3 | None | application | mathematics | 'Sage is a free open-source mathematics software system licensed under the GPL. It builds on top of many existing open-source packages: NumPy, SciPy, matplotlib, Sympy, Maxima, GAP, FLINT, R and many more.' Mission: 'Creating a viable free open source alternative to Magma, Maple, Mathematica and Matlab.' |
salmon | 0.6.0 | salmon/0.6 | None | application | computational biology | Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using lightweight alignments. |
salmon | 0.8.2 | salmon/0.8 | None | application | computational biology | Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using lightweight alignments. |
salmon | 0.9.1 | salmon/0.9 | None | application | computational biology | Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using lightweight alignments. |
salmon | 1.4.0 | salmon/1.4 | None | application | computational biology | Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using lightweight alignments. |
salsa2 | 2.3 | salsa2/2.3 | None | application | bioinformatics | Salsa is a tool to scaffold long read assemblies with Hi-C. |
sambamba | 0.8.1 | sambamba/0.8 | None | application | Bioinformatics | Tools for working with SAM/BAM data |
samtools | 0.1 | samtools/0.1 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.15.1 | samtools/1.15 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.17 | samtools/1.17 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.19 | samtools/1.19 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.20 | samtools/1.20 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.3 | samtools/1.3 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.5 | samtools/1.5 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.6 | samtools/1.6 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
samtools | 1.9 | samtools/1.9 | None | application | computational biology | Tools for dealing with SAM, BAM and CRAM files |
sas | 9.4 | sas/9.4 | None | application | Applications | SAS is a software suite developed by SAS Institute for advanced analytics, business intelligence, data management, and predictive analytics. |
scaffold_builder | 2.2 | scaffold_builder/2.2 | None | application | computational biology | Scaffold_builder: Combining de novo and reference-guided assembly with Scaffold_builder. |
scan-for-matches | 1.0 | scan-for-matches/1.0 | None | application | computational biology | scan_for_matches is a utility written in C for locating patterns in DNA or protein FASTA files. |
schrodinger | 2020.1 | schrodinger/2020.1 | None | application | Simulation | Schrödinger is the scientific leader in developing state-of-the-art chemical simulation software for use in pharmaceutical, biotechnology, and materials research. |
schrodinger | 2020.4 | schrodinger/2020.4 | None | application | Simulation | Schrödinger is the scientific leader in developing state-of-the-art chemical simulation software for use in pharmaceutical, biotechnology, and materials research. |
schrodinger | 2021.1 | schrodinger/2021.1 | None | application | Simulation | Schrödinger is the scientific leader in developing state-of-the-art chemical simulation software for use in pharmaceutical, biotechnology, and materials research. |
schrodinger | 2022.1 | schrodinger/2022.1 | None | application | Simulation | Schrödinger is the scientific leader in developing state-of-the-art chemical simulation software for use in pharmaceutical, biotechnology, and materials research. |
scip | 4.0.0 | scip/4.0 | None | application | constraint integer programming | SCIP is currently one of the fastest non-commercial solvers for mixed integer programming (MIP) and mixed integer nonlinear programming (MINLP). |
scoary | 1.6.16 | scoary/py27/1.6 | None | application | computational biology | Microbial pan-GWAS using the output from Roary |
scoary | 1.6.16 | scoary/py35/1.6 | None | application | computational biology | Microbial pan-GWAS using the output from Roary |
scoary | 1.6.16 | scoary/py36/1.6 | None | application | computational biology | Microbial pan-GWAS using the output from Roary |
scons | 2.5 | scons/2.5 | None | application | utility | SCons: A software construction tool. |
scons | 3.0 | scons/3.0 | None | application | utility | SCons: A software construction tool. |
scons | 3.1.2 | scons/py27/3.1 | None | application | utility | SCons: A software construction tool. |
scons | 3.1.2 | scons/py38/3.1 | None | application | utility | SCons: A software construction tool. |
scons | 3.1.2 | scons/py39/3.1 | None | application | utility | SCons: A software construction tool. |
scons | 4.2.0 | scons/py37/4.2 | None | application | utility | SCons: A software construction tool. |
scons | 4.2.0 | scons/py38/4.2 | None | application | utility | SCons: A software construction tool. |
scons | 4.2.0 | scons/py39/4.2 | None | application | utility | SCons: A software construction tool. |
scons | 4.3.0 | scons/py37/4.3 | None | application | utility | SCons: A software construction tool. |
scons | 4.3.0 | scons/py38/4.3 | None | application | utility | SCons: A software construction tool. |
scons | 4.3.0 | scons/py39/4.3 | None | application | utility | SCons: A software construction tool. |
scythe | 0.991 | scythe/0.991 | None | application | bioinformatics | A 3'-end adapter contaminant trimmer. |
seacr | 1.3 | seacr/1.3 | None | application | computational biology | SEACR is Sparse Enrichment Analysis for CUT&RUN |
seedme | 1.2 | seedme/1.2 | None | application | Utility | Client program for SeedMe.org. |
selecton | 2.4 | selecton/2.4 | None | application | Bioinformatics | Selecton 2007: advanced models for detecting positive and purifying selection using a Bayesian inference approach. |
sepp | 1.0 | sepp/1.0 | None | library | runtime support | |
seqkit | 0.10.1 | seqkit/0.10 | None | application | computational biology | Cross-platform and ultrafast toolkit for FASTA/Q file manipulation |
seqkit | 2.6.1 | seqkit/2.6 | None | application | computational biology | Cross-platform and ultrafast toolkit for FASTA/Q file manipulation |
seqtk | 1.2 | seqtk/1.2 | None | application | computational biology | Seqtk is a fast and lightweight tool for processing sequences in the FASTA or FASTQ format. |
seqyclean | 1.10.07 | seqyclean/1.10 | None | application | Bioinformatics | Main purpose of this software is to pre-process NGS data in order to prepare for downstream analysis. |
settarg | None | settarg | None | unknown | unknown | The settarg module provides a way to connect the loaded modules with your build system by setting environment variables. |
settarg | settarg | settarg/settarg | None | unknown | unknown | The settarg module provides a way to connect the loaded modules with your build system by setting environment variables. |
sff2fastq | 0.9.2 | sff2fastq/0.9 | None | application | computational biology | The program sff2fastq extracts read information from a SFF file, produced by the 454 genome sequencer, and outputs the sequences and quality scores in a FASTQ format. |
shapeit | 2.0 | shapeit/2.0 | None | application | computational biology | SHAPEIT is a fast and accurate method for estimation of haplotypes (aka phasing) from genotype or sequencing data. |
shapeit | 5.1.1 | shapeit/5.1 | None | application | computational biology | SHAPEIT is a fast and accurate method for estimation of haplotypes (aka phasing) from genotype or sequencing data. |
shapelib | 1.5.0 | shapelib/1.5 | compiler/intel/20 compiler/gcc/9 compiler/pgi/20 compiler/intel/19 compiler/gcc/10 | library | runtime support | The Shapefile C Library provides the ability to write simple C programs for reading, writing and updating (to a limited extent) ESRI Shapefiles, and the associated attribute file (.dbf). |
shasta | 0.11.1 | shasta/0.11 | None | application | Bioinformatics | De novo assembly from Oxford Nanopore reads. |
shasta | 0.8.0 | shasta/0.8 | None | application | Bioinformatics | De novo assembly from Oxford Nanopore reads. |
shortbred | 0.9.5 | shortbred/0.9 | None | application | bioinformatics | ShortBRED is a system for profiling protein families of interest at very high specificity in shotgun metagenomic sequencing data. |
shortstack | 3.8.5 | shortstack/3.8 | None | application | Biology | ShortStack: Comprehensive annotation and quantification of small RNA genes |
shovill | 1.0.9 | shovill/1.0 | None | application | computational biology | Microbial assembly pipeline for Illumina paired-end reads |
shrimp | 2.2 | shrimp/2.2 | None | application | computational biology | SHRiMP is a software package for aligning genomic reads against a target genome. |
shtns | 2.6.3 | shtns/py36/2.6 | None | application | high performance library | SHTns is a high performance library for Spherical Harmonic Transform written in C, aimed at numerical simulation (fluid flows, mhd, ...) in spherical geometries. |
shtns | 2.6.3 | shtns/py310/2.6 | None | application | high performance library | SHTns is a high performance library for Spherical Harmonic Transform written in C, aimed at numerical simulation (fluid flows, mhd, ...) in spherical geometries. |
shtns | 3.6 | shtns/py36/3.6 | None | application | high performance library | SHTns is a high performance library for Spherical Harmonic Transform written in C, aimed at numerical simulation (fluid flows, mhd, ...) in spherical geometries. |
shtns | 3.6 | shtns/py310/3.6 | None | application | high performance library | SHTns is a high performance library for Spherical Harmonic Transform written in C, aimed at numerical simulation (fluid flows, mhd, ...) in spherical geometries. |
sicerpy | 0.1.1 | sicerpy/0.1 | None | application | Biology | Python wrapper around the popular ChIP-Seq peak caller SICER. |
sickle | 1.2 | sickle/1.210 | None | application | computational biology | A windowed adaptive trimming tool for FASTQ files using quality |
sickle | 1.33 | sickle/1.33 | None | application | computational biology | A windowed adaptive trimming tool for FASTQ files using quality |
sift4g | 2.0.0 | sift4g/2.0 | None | application | computational biology | SIFT 4G is a faster version of SIFT that enables us to scale up and provide SIFT predictions for more organisms. |
signalp | 4.1 | signalp/4.1 | None | application | Biology | signalp predicts the presence and location of signal peptide cleavage sites in amino acid sequences from different organisms: Gram-positive bacteria, Gram-negative bacteria, and eukaryotes. |
signalp | 5.0b | signalp/5.0b | None | application | Biology | signalp predicts the presence and location of signal peptide cleavage sites in amino acid sequences from different organisms: Gram-positive bacteria, Gram-negative bacteria, and eukaryotes. |
simrna | 3.20 | simrna/3.20 | None | application | computational biology | SimRNA is a tool for simulations of RNA conformational dynamics |
singularity | 3.8 | singularity/2.2 | None | application | system | Application containers enabling mobility of compute. |
singularity | 3.8 | singularity/2.3 | None | application | system | Application containers enabling mobility of compute. |
singularity | 3.8 | singularity/2.4 | None | application | system | Application containers enabling mobility of compute. |
singularity | 3.8 | singularity/2.6 | None | application | system | Application containers enabling mobility of compute. |
singularity | 3.8 | singularity/3.2 | None | application | system | Application containers enabling mobility of compute. |
singularity | 3.8 | singularity/3.8 | None | application | system | Application containers enabling mobility of compute. |
sistr_cmd | 1.0.2 | sistr_cmd/1.0 | None | application | computational biology | Salmonella In Silico Typing Resource command-line tool |
sistr_cmd | 1.1.1 | sistr_cmd/1.1 | None | application | computational biology | Salmonella In Silico Typing Resource command-line tool |
smetana | 1.2.0 | smetana/py36/1.2 | None | application | genomics | Species METabolic interaction ANAlysis (SMETANA) is a python-based command line tool to analyse microbial communities. |
smrtlink | 10.1.0.119588 | smrtlink/10.1 | None | application | Biology | PacBio's open-source SMRT Analysis software suite is designed for use with Single Molecule, Real-Time (SMRT) Sequencing data. |
smrtlink | 5.0.1 | smrtlink/5.0 | None | application | Biology | PacBio's open-source SMRT Analysis software suite is designed for use with Single Molecule, Real-Time (SMRT) Sequencing data. |
smrtlink | 5.1.0.26412 | smrtlink/5.1 | None | application | Biology | PacBio's open-source SMRT Analysis software suite is designed for use with Single Molecule, Real-Time (SMRT) Sequencing data. |
smrtlink | 7.0.1.66975 | smrtlink/7.0 | None | application | Biology | PacBio's open-source SMRT Analysis software suite is designed for use with Single Molecule, Real-Time (SMRT) Sequencing data. |
snakemake | 5.18.0 | snakemake/5.18 | None | application | Utility | A popular workflow management system aiming at full in-silico reproducibility. |
snakemake | 6.4.1 | snakemake/6.4 | None | application | Utility | A popular workflow management system aiming at full in-silico reproducibility. |
snap | 2013-11-29 | snap/2013-11-29 | None | application | computational biology | SNAP - (Semi-HMM-based Nucleic Acid Parser) gene prediction tool. |
sniffles | 1.0.12 | sniffles/1.0 | None | application | computational biology | Sniffles is a structural variation caller using third generation sequencing (PacBio or Oxford Nanopore) |
sniffles | 2.4 | sniffles/2.4 | None | application | computational biology | Sniffles is a structural variation caller using third generation sequencing (PacBio or Oxford Nanopore) |
snippy | 4.3.6 | snippy/4.3 | None | application | computational biology | Rapid bacterial SNP calling and core genome alignments |
snippy | 4.6.0 | snippy/4.6 | None | application | computational biology | Rapid bacterial SNP calling and core genome alignments |
snp-dists | 0.6.3 | snp-dists/0.6 | None | application | computational biology | Convert a FASTA alignment to SNP distance matrix |
snp-dists | 0.7.0 | snp-dists/0.7 | None | application | computational biology | Convert a FASTA alignment to SNP distance matrix |
snp-dists | 0.8.2 | snp-dists/0.8 | None | application | computational biology | Convert a FASTA alignment to SNP distance matrix |
snp-pipeline | 0.6 | snp-pipeline/0.6 | None | application | computational biology | Script and functions for SNP matrix construction |
snp-pipeline | 0.7 | snp-pipeline/0.7 | None | application | computational biology | Script and functions for SNP matrix construction |
snp-pipeline | 1.0 | snp-pipeline/1.0 | None | application | computational biology | Script and functions for SNP matrix construction |
snp-pipeline | 2.0.2 | snp-pipeline/2.0 | None | application | computational biology | Script and functions for SNP matrix construction |
snp-sites | 2.3.3 | snp-sites/2.3 | None | application | computational biology | SNP-sites rapidly extracts SNPs from a multi-FASTA alignment. |
snp-sites | 2.4.1 | snp-sites/2.4 | None | application | computational biology | SNP-sites rapidly extracts SNPs from a multi-FASTA alignment. |
snp-sites | 2.5.1 | snp-sites/2.5 | None | application | computational biology | SNP-sites rapidly extracts SNPs from a multi-FASTA alignment. |
snpeff | 4.3 | snpeff/4.3 | None | application | computational biology | Genetic variant annotation and effect prediction toolbox. |
snpeff | 5.1 | snpeff/5.1 | None | application | computational biology | Genetic variant annotation and effect prediction toolbox. |
snpfinder | 1.0.0 | snpfinder/1.0 | None | application | computational biology | SNPFinder is a simple alignment-based haplotype variant caller that can be used with metagenomic sequence data. |
snptest | 2.5.2 | snptest/2.5 | None | application | computational biology | SNPTEST is a program for the analysis of single SNP association in genome-wide studies. |
soapdenovo-trans | 1.04 | soapdenovo-trans/1.04 | None | application | computational biology | SOAPdenovo-Trans is a de novo transcriptome assembler basing on the SOAPdenovo framework, adapt to alternative splicing and different expression level among transcripts. |
soapdenovo2 | r240 | soapdenovo2/r240 | None | application | computational biology | soapdenovo2 - novel short-read assembly method that can build a de novo draft assembly for the human-sized genomes |
sonnet | 1.19 | sonnet/py27/1.19 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 1.19 | sonnet/py35/1.19 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 1.19 | sonnet/py36/1.19 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 1.23 | sonnet/py27/1.23 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 1.23 | sonnet/py35/1.23 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 1.23 | sonnet/py36/1.23 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 1.27 | sonnet/py27/1.27 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 1.27 | sonnet/py36/1.27 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 2.0.0 | sonnet/py38/2.0 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet | 2.0.0 | sonnet/py39/2.0 | None | application | machine learning | Sonnet is a library built on top of TensorFlow 2 designed to provide simple, composable abstractions for machine learning research. |
sonnet-gpu | 1.19 | sonnet-gpu/py27/1.19 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sonnet-gpu | 1.19 | sonnet-gpu/py35/1.19 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sonnet-gpu | 1.19 | sonnet-gpu/py36/1.19 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sonnet-gpu | 1.23 | sonnet-gpu/py27/1.23 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sonnet-gpu | 1.23 | sonnet-gpu/py35/1.23 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sonnet-gpu | 1.23 | sonnet-gpu/py36/1.23 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sonnet-gpu | 1.27 | sonnet-gpu/py27/1.27 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sonnet-gpu | 1.27 | sonnet-gpu/py36/1.27 | None | application | machine learning | Sonnet is a library built on top of TensorFlow for building complex neural networks. |
sortmerna | 4.3.2 | sortmerna/4.3.2 | None | application | biological sequence analysis | SortMeRNA is a biological sequence analysis tool for filtering, mapping and OTU-picking NGS reads. |
spacy | 2.2.3 | spacy/py36/2.2 | None | application | deep learning | Industrial-strength Natural Language Processing |
spacy | 2.2.3 | spacy/py37/2.2 | None | application | deep learning | Industrial-strength Natural Language Processing |
spacy-gpu | 2.2.4 | spacy-gpu/py36/2.2 | None | application | deep learning | Industrial-strength Natural Language Processing |
spacy-gpu | 2.2.4 | spacy-gpu/py37/2.2 | None | application | deep learning | Industrial-strength Natural Language Processing |
spades | 3.10.1 | spades/3.10 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.11.1 | spades/3.11 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.12.0 | spades/3.12 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.13.0 | spades/py27/3.13 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.13.0 | spades/py35/3.13 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.13.0 | spades/py36/3.13 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.14.0 | spades/3.14 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.15.2 | spades/3.15 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
spades | 3.8.1 | spades/3.8 | None | application | computational biology | SPAdes - St. Petersburg genome assembler - is intended for both standard isolates and single-cell MDA bacteria assemblies. |
sparcc | 0.1.0 | sparcc/py27/0.1 | None | application | computational biology | SparCC is a python module for computing correlations in compositional data (16S, metagenomics, etc). |
sparta | 18Jul2022 | sparta/18Jul2022 | compiler/gcc/11:openmpi/4.1 | application | Simulation | Stochastic PArallel Rarefied-gas Time-accurate Analyzer. |
spglib | 2.0.2 | spglib/2.0 | compiler/intel/20 | library | runtime support | |
spider | 2.0 | spider/2.0 | None | application | computational biology | Sequence-based Prediction of Local and Nonlocal Structural Features for Proteins. |
spirit | 2.1.1 | spirit/py36/2.1 | None | application | Physics | Optimizations and Dynamics Framework for atomistic Spin systems |
spirit | 2.1.1 | spirit/py37/2.1 | None | application | Physics | Optimizations and Dynamics Framework for atomistic Spin systems |
spirit | 2.1.1 | spirit/py38/2.1 | None | application | Physics | Optimizations and Dynamics Framework for atomistic Spin systems |
spirit-gpu | 2.1.1 | spirit-gpu/py36/2.1 | None | application | Physics | Optimizations and Dynamics Framework for atomistic Spin systems |
spirit-gpu | 2.1.1 | spirit-gpu/py37/2.1 | None | application | Physics | Optimizations and Dynamics Framework for atomistic Spin systems |
spirit-gpu | 2.1.1 | spirit-gpu/py38/2.1 | None | application | Physics | Optimizations and Dynamics Framework for atomistic Spin systems |
spm | 12 | spm/12 | compiler/gcc/11 | application | matlab toolbox | Statistical Parametric Mapping refers to the construction and assessment of spatially extended statistical processes used to test hypotheses about functional imaging data. |
spp | 1.11 | spp/1.11 | None | application | computational biology | ChIP-seq peak caller |
spp | 1.13 | spp/1.13 | None | application | computational biology | ChIP-seq peak caller |
spython | 0.0.69 | spython/0.0.69 | None | application | singularity | Command line python tool for working with singularity. |
sqlite | 3.33.0 | sqlite/3.33 | compiler/gcc/10 compiler/intel/20 compiler/pgi/20 compiler/intel/19 compiler/gcc/9 compiler/gcc/11 | library | runtime support | |
ssages | 0.9.3 | ssages/0.9gromacs | compiler/gcc/9:openmpi/4.0 | application | molecular dynamics | |
ssages | 0.9.3 | ssages/0.9lammps | compiler/gcc/9:openmpi/4.0 | application | molecular dynamics | |
ssake | 4.0 | ssake/4.0 | None | application | genomics | SSAKE is a genomics application for de novo assembly of millions of very short DNA sequences. |
stacks | 2.4 | stacks/2.4 | None | application | computational biology | Stacks is a software pipeline for building loci from RAD-seq |
stamp | 2.1.3 | stamp/2.1 | None | application | Taxonomy | A graphical software package for analyzing taxonomic and functional profiles. |
staphb-toolkit | 1.3.6 | staphb-toolkit/1.3 | None | application | Bioinformatics | The StaPH-B ToolKit is a Python library of commonly used bioinformatics tools that help to inform public health action. The StaPH-B ToolKit utilizes the StaPH-B Docker Images to enable easy access of open-source software without the need of local installation and/or dependency maintenance. |
staphb-toolkit | 20200304 | staphb-toolkit/20200304 | None | application | Bioinformatics | The StaPH-B ToolKit is a Python library of commonly used bioinformatics tools that help to inform public health action. The StaPH-B ToolKit utilizes the StaPH-B Docker Images to enable easy access of open-source software without the need of local installation and/or dependency maintenance. |
star | 2.7.11b | star/2.7 | None | application | biology | An RNA-seq read aligner. |
star | 2.7.9a | star/2.7.9a | None | application | biology | An RNA-seq read aligner. |
star-fusion | 1.13.0 | star-fusion/1.13 | None | application | computational biology | STAR-Fusion fusion variant caller. |
star-fusion | 1.9.0 | star-fusion/1.9 | None | application | computational biology | STAR-Fusion fusion variant caller. |
starccm | 10.01.010 | starccm/10.06 | None | library | runtime support | |
starccm | 9.01.011 | starccm/9.06 | None | library | runtime support | |
starship | 1.20.1 | starship/1.20 | None | application | Cross-shell prompt | The minimal, blazing-fast, and infinitely customizable prompt for any shell! |
stereogene | 2.20 | stereogene/2.20 | None | application | sequencing | StereoGene: Rapid Estimation of Genomewide Correlation of Continuous or Interval Feature Data |
strainest | 1.2.4 | strainest/1.2 | None | application | Biology | Abundance estimation of strains |
strelka | 2.9.10 | strelka/2.9 | None | application | computational biology | Strelka calls somatic and germline small variants from mapped sequencing reads |
stringmlst | 0.6.3 | stringmlst/0.6 | None | application | computational biology | Fast k-mer based tool for multi locus sequence typing (MLST) directly from genome sequencing reads |
structure | 2.3.4 | structure/2.3 | None | application | computational biology | The program structure is a free software package for using multi-locus genotype data to investigate population structure. Its uses include inferring the presence of distinct populations, assigning individuals to populations, studying hybrid zones, identifying migrants and admixed individuals, and estimating population allele frequencies in situations where many individuals are migrants or admixed. It can be applied to most of the commonly-used genetic markers, including SNPS, microsatellites, RFLPs and AFLPs. |
subread | 1.4.6p5 | subread/1.4 | None | application | computational biology | The Subread package is developed in The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia. It consists of a suite of programs for processing next-gen sequencing data. |
subread | 2.0.0 | subread/2.0 | None | application | computational biology | The Subread package is developed in The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia. It consists of a suite of programs for processing next-gen sequencing data. |
subversion | 1.10.8 | subversion/1.10 | None | library | tools | Enterprise-class centralized version control for the masses |
subversion | 1.14.2 | subversion/1.14 | None | library | tools | Enterprise-class centralized version control for the masses |
suitesparse | 5.10.1 | suitesparse/5.10 | compiler/gcc/10 | library | runtime support | SuiteSparse: A Suite of Sparse matrix packages. |
svn | 1.10.8 | svn/1.10 | None | library | tools | Enterprise-class centralized version control for the masses |
svn | 1.14.2 | svn/1.14 | None | library | tools | Enterprise-class centralized version control for the masses |
svsolver | 2022.07.20 | svsolver/2022.07.20 | compiler/gcc/10:openmpi/4.1 | application | Biology | The svSolver includes three executable programs: Presolver(svpre), Flowsolver(svsolver), Postsolver(svpost). |
swan | None | swan | None | unknown | unknown | |
sweepfinder2 | 1.0 | sweepfinder2/1.0 | None | application | Biology | The BWA read mapper. |
szip | 2.1 | szip/2.1 | compiler/gcc/9 compiler/gcc/11 compiler/gcc/10 compiler/intel/18 | library | runtime support | |
szip | 2.1.1 | szip/2.1 | compiler/intel/19 compiler/pgi/20 compiler/intel/20 | library | runtime support | |
t-coffee | 13.39.0.d675aed | t-coffee/13.39 | None | application | computational biology | A collection of tools for Multiple Alignments of DNA, RNA, Protein Sequence |
t-coffee | 13.45.0.4846264 | t-coffee/13.45 | None | application | computational biology | A collection of tools for Multiple Alignments of DNA, RNA, Protein Sequence |
tabix | 0.2.6 | tabix/0.2 | None | application | computational biology | A set of tools written in Perl and C++ for working with VCF files. |
tagcleaner | 0.16 | tagcleaner/0.16 | None | application | computational biology | The TagCleaner tool can be used to automatically detect and efficiently remove tag sequences (e.g. WTA tags) from genomic and metagenomic datasets. It is easily configurable and provides a user-friendly interface. |
targetfinder | 1.7 | targetfinder/1.7 | None | application | computational biology | Plant small RNA target prediction tool. |
tassel | 3.0 | tassel/3.0 | None | application | computational biology | TASSEL is a software package to evaluate traits associations, evolutionary patterns, and linkage disequilibrium. |
tassel | 4.0 | tassel/4.0 | None | application | computational biology | TASSEL is a software package to evaluate traits associations, evolutionary patterns, and linkage disequilibrium. |
tassel | 5.1 | tassel/5.1 | None | application | computational biology | TASSEL is a software package to evaluate traits associations, evolutionary patterns, and linkage disequilibrium. |
tassel | 5.2.89 | tassel/5.2 | None | application | computational biology | TASSEL is a software package to evaluate traits associations, evolutionary patterns, and linkage disequilibrium. |
tax2tree | 1.0 | tax2tree/1.0 | None | application | computational biology | tax2tree - Tools for decorating taxonomy information on to a phylogenetic tree. |
taxypro | 1.0 | taxypro/1.0 | None | application | mixture modeling for taxonomic analysis of metagenomes | |
taxytoolbox | 1.0 | taxytoolbox/1.0 | None | application | mixture modeling for taxonomic analysis of metagenomes | |
tciaclient | 0.0.3 | tciaclient/py38/0.0.3 | None | application | TCIA | TCIA (The Cancer Imaging Archive) Download Client for Python |
tensorflow | 0.12.1 | tensorflow/py27/0.12 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 0.12.1 | tensorflow/py35/0.12 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.0.0 | tensorflow/py27/1.0 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.0.0 | tensorflow/py35/1.0 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.11.0 | tensorflow/py27/1.11 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.11.0 | tensorflow/py36/1.11 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.12.0 | tensorflow/py27/1.12 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.12.0 | tensorflow/py36/1.12 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.14.0 | tensorflow/py27/1.14 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.14.0 | tensorflow/py36/1.14 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.14.0 | tensorflow/py37/1.14 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.3.1 | tensorflow/py27/1.3 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.3.1 | tensorflow/py35/1.3 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.3.1 | tensorflow/py36/1.3 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.4.0 | tensorflow/py27/1.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.4.0 | tensorflow/py35/1.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.4.0 | tensorflow/py36/1.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.5.0 | tensorflow/py27/1.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.5.0 | tensorflow/py35/1.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.5.0 | tensorflow/py36/1.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.7.0 | tensorflow/py27/1.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.7.0 | tensorflow/py35/1.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 1.7.0 | tensorflow/py36/1.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.0.0 | tensorflow/py36/2.0 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.0.0 | tensorflow/py37/2.0 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.1.0 | tensorflow/py36/2.1 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.1.0 | tensorflow/py37/2.1 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.10.0 | tensorflow/py38/2.10 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.10.0 | tensorflow/py39/2.10 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.11.0 | tensorflow/py38/2.11 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.11.0 | tensorflow/py39/2.11 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.15.0 | tensorflow/py310/2.15 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.15.0 | tensorflow/py311/2.15 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.2.0 | tensorflow/py36/2.2 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.2.0 | tensorflow/py37/2.2 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.3.0 | tensorflow/py37/2.3 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.3.0 | tensorflow/py38/2.3 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.4.1 | tensorflow/py37/2.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.4.1 | tensorflow/py38/2.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.4.1 | tensorflow/py39/2.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.5.0 | tensorflow/py37/2.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.5.0 | tensorflow/py38/2.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.5.0 | tensorflow/py39/2.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.6.0 | tensorflow/py38/2.6 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.6.0 | tensorflow/py39/2.6 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.7.0 | tensorflow/py38/2.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.7.0 | tensorflow/py39/2.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.8.2 | tensorflow/py38/2.8 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.8.2 | tensorflow/py39/2.8 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.9.1 | tensorflow/py38/2.9 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow | 2.9.1 | tensorflow/py39/2.9 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.12.0 | tensorflow-gpu/py27/1.12 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.12.0 | tensorflow-gpu/py36/1.12 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.13.1 | tensorflow-gpu/py27/1.13 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.13.1 | tensorflow-gpu/py36/1.13 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.13.1 | tensorflow-gpu/py37/1.13 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.14.0 | tensorflow-gpu/py27/1.14 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.14.0 | tensorflow-gpu/py36/1.14 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.14.0 | tensorflow-gpu/py37/1.14 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.5.0 | tensorflow-gpu/py27/1.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.5.0 | tensorflow-gpu/py35/1.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.5.0 | tensorflow-gpu/py36/1.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.7.0 | tensorflow-gpu/py27/1.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.7.0 | tensorflow-gpu/py35/1.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 1.7.0 | tensorflow-gpu/py36/1.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.0.0 | tensorflow-gpu/py36/2.0 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.0.0 | tensorflow-gpu/py37/2.0 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.1.0 | tensorflow-gpu/py36/2.1 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.1.0 | tensorflow-gpu/py37/2.1 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.10.0 | tensorflow-gpu/py38/2.10 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.10.0 | tensorflow-gpu/py39/2.10 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.11.0 | tensorflow-gpu/py38/2.11 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.11.0 | tensorflow-gpu/py39/2.11 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.15.0 | tensorflow-gpu/py310/2.15 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.15.0 | tensorflow-gpu/py311/2.15 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.2.0 | tensorflow-gpu/py36/2.2 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.2.0 | tensorflow-gpu/py37/2.2 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.3.0 | tensorflow-gpu/py38/2.3 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.4.1 | tensorflow-gpu/py38/2.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.4.1 | tensorflow-gpu/py39/2.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.5.0 | tensorflow-gpu/py37/2.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.5.0 | tensorflow-gpu/py38/2.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.5.0 | tensorflow-gpu/py39/2.5 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.6.0 | tensorflow-gpu/py38/2.6 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.6.0 | tensorflow-gpu/py39/2.6 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.7.0 | tensorflow-gpu/py38/2.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.7.0 | tensorflow-gpu/py39/2.7 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.8.1 | tensorflow-gpu/py38/2.8 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.8.1 | tensorflow-gpu/py39/2.8 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.9.1 | tensorflow-gpu/py38/2.9 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | 2.9.1 | tensorflow-gpu/py39/2.9 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | py37/2.3 | tensorflow-gpu/py37/2.3 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tensorflow-gpu | py37/2.4 | tensorflow-gpu/py37/2.4 | None | application | machine learning | TensorFlow is an open source software library for numerical computation using data flow graphs. |
tf-comb | 1.0.3 | tf-comb/py38/1.0 | None | application | Bioinformatics | Transcription Factor Co-Occurrence using Market Basket analysis |
tf-comb | 1.0.3 | tf-comb/py39/1.0 | None | application | Bioinformatics | Transcription Factor Co-Occurrence using Market Basket analysis |
tf-comb | 1.0.3 | tf-comb/py310/1.0 | None | application | Bioinformatics | Transcription Factor Co-Occurrence using Market Basket analysis |
tf-comb | 1.1 | tf-comb/py38/1.1 | None | application | Bioinformatics | Transcription Factor Co-Occurrence using Market Basket analysis |
tf-comb | 1.1 | tf-comb/py39/1.1 | None | application | Bioinformatics | Transcription Factor Co-Occurrence using Market Basket analysis |
tf-comb | 1.1 | tf-comb/py310/1.1 | None | application | Bioinformatics | Transcription Factor Co-Occurrence using Market Basket analysis |
theano | 0.9.0 | theano/py27/0.9 | None | application | mathematics | Theano is a Python library that allows you to define, optimize, and evaluate mathematical expressions involving multi-dimensional arrays efficiently. |
theano | 0.9.0 | theano/py35/0.9 | None | application | mathematics | Theano is a Python library that allows you to define, optimize, and evaluate mathematical expressions involving multi-dimensional arrays efficiently. |
theano | 0.9.0 | theano/py36/0.9 | None | application | mathematics | Theano is a Python library that allows you to define, optimize, and evaluate mathematical expressions involving multi-dimensional arrays efficiently. |
theano | 1.0.3 | theano/py27/1.0 | None | application | mathematics | Theano is a Python library that allows you to define, optimize, and evaluate mathematical expressions involving multi-dimensional arrays efficiently. |
theano | 1.0.3 | theano/py35/1.0 | None | application | mathematics | Theano is a Python library that allows you to define, optimize, and evaluate mathematical expressions involving multi-dimensional arrays efficiently. |
theano | 1.0.3 | theano/py36/1.0 | None | application | mathematics | Theano is a Python library that allows you to define, optimize, and evaluate mathematical expressions involving multi-dimensional arrays efficiently. |
tmhmm | 2.0c | tmhmm/2.0c | None None | application | computational biology | TMHMM 2.0 predicts transmembrane helices in proteins. |
tobias | 0.13.3 | tobias/py37/0.13 | None | application | computational biology | Transcription factor Occupancy prediction By Investigation of ATAC-seq Signal |
topas-mc | 3.9 | topas-mc/3.9 | None | application | Physics | TOPAS: Tool for Particle Simulation |
tophat | 2.0.14 | tophat/2.0 | None | application | computational biology | TopHat2 is a fast splice junction mapper for RNA-Seq reads. It aligns RNA-Seq reads to mammalian-sized genomes using the ultra high-throughput short read aligner Bowtie, and then analyzes the mapping results to identify splice junctions between exons. |
tophat | 2.1.1 | tophat/2.1 | None | application | computational biology | TopHat2 is a fast splice junction mapper for RNA-Seq reads. It aligns RNA-Seq reads to mammalian-sized genomes using the ultra high-throughput short read aligner Bowtie, and then analyzes the mapping results to identify splice junctions between exons. |
tpmcalculator | 0.0.4 | tpmcalculator/0.0.4 | None | application | bioinformatics | TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files. |
transcriptm | 0.2 | transcriptm/0.2 | None | application | bioinformatics | Metagenomics analyses. |
transdecoder | 2.0.1 | transdecoder/2.0 | None | application | computational biology | TransDecoder identifies candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to the genome using Tophat and Cufflinks. |
transdecoder | 3.0.1 | transdecoder/3.0 | None | application | computational biology | TransDecoder identifies candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to the genome using Tophat and Cufflinks. |
transformers | 4.31.0 | transformers/py39/4.31 | None | application | machine learning | State-of-the-art Natural Language Processing for TensorFlow 2.0 and PyTorch |
transformers | 4.31.0 | transformers/py310/4.31 | None | application | machine learning | State-of-the-art Natural Language Processing for TensorFlow 2.0 and PyTorch |
transformers-gpu | 4.31.0 | transformers-gpu/py39/4.31 | None | application | machine learning | State-of-the-art Natural Language Processing for TensorFlow 2.0 and PyTorch |
transformers-gpu | 4.31.0 | transformers-gpu/py310/4.31 | None | application | machine learning | State-of-the-art Natural Language Processing for TensorFlow 2.0 and PyTorch |
transrate | 0.1 | transrate/0.1 | None | application | life sciences | transrate - Quality assessment and comparison of transcriptome assemblies |
treemix | 1.12 | treemix/1.12 | None | application | computational biology | TreeMix is a method for inferring the patterns of population splits and mixtures in the history of a set of populations. |
treemix | 1.13 | treemix/1.13 | None | application | computational biology | TreeMix is a method for inferring the patterns of population splits and mixtures in the history of a set of populations. |
trf | 4.07b | trf/4.0 | None | application | computational biology | Tandem Repeats Finder is a program to locate and display tandem repeats in DNA sequences. |
triform2 | 0.0.5 | triform2/0.0.5 | None | application | computational biology | Improved sensitivity, specificity and control of false discovery rates in ChIP-Seq peak finding. |
trim_galore | 0.4.5 | trim_galore/0.4 | None | application | computational biology | Trim Galore! is a wrapper script to automate quality and adapter trimming as well as quality control |
trim_galore | 0.6.5 | trim_galore/0.6 | None | application | computational biology | Trim Galore! is a wrapper script to automate quality and adapter trimming as well as quality control |
trimmomatic | 0.33 | trimmomatic/0.33 | None | application | computational biology | A flexible read trimming tool for Illumina NGS data |
trimmomatic | 0.36 | trimmomatic/0.36 | None | application | computational biology | A flexible read trimming tool for Illumina NGS data |
trimmomatic | 0.38 | trimmomatic/0.38 | None | application | computational biology | A flexible read trimming tool for Illumina NGS data |
trimmomatic | 0.39 | trimmomatic/0.39 | None | application | computational biology | A flexible read trimming tool for Illumina NGS data |
trinity | 2.11.0 | trinity/2.11 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | 2.12.0 | trinity/2.12 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | 2.13.2 | trinity/2.13 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | 2.15.1 | trinity/2.15 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | 2.4.0 | trinity/2.4 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | 2.6.6 | trinity/2.6 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | 2.8.4 | trinity/2.8 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | 2.9.1 | trinity/2.9 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | r2013-11-10 | trinity/r2013-11-10 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinity | r2014-04-13p1 | trinity/r2014-04-13p1 | None | application | computational biology | Trinity RNA-Seq de novo transcriptome assembly |
trinotate | 2.0.2 | trinotate/2.0 | None | application | computational biology | Trinotate is a comprehensive annotation suite designed for automatic functional annotation of transcriptomes, particularly de novo assembled transcriptomes, from model or non-model organisms. Trinotate makes use of a number of different well referenced methods for functional annotation including homology search to known sequence data (BLAST+/SwissProt), protein domain identification (HMMER/PFAM), protein signal peptide and transmembrane domain prediction (signalP/tmHMM), and leveraging various annotation databases (eggNOG/GO/Kegg databases). All functional annotation data derived from the analysis of transcripts is integrated into a SQLite database which allows fast efficient searching for terms with specific qualities related to a desired scientific hypothesis or a means to create a whole annotation report for a transcriptome. |
trinotate | 3.2.1 | trinotate/3.2 | None | application | computational biology | Trinotate is a comprehensive annotation suite designed for automatic functional annotation of transcriptomes, particularly de novo assembled transcriptomes, from model or non-model organisms. Trinotate makes use of a number of different well referenced methods for functional annotation including homology search to known sequence data (BLAST+/SwissProt), protein domain identification (HMMER/PFAM), protein signal peptide and transmembrane domain prediction (signalP/tmHMM), and leveraging various annotation databases (eggNOG/GO/Kegg databases). All functional annotation data derived from the analysis of transcripts is integrated into a SQLite database which allows fast efficient searching for terms with specific qualities related to a desired scientific hypothesis or a means to create a whole annotation report for a transcriptome. |
trinotate | r2013-11-10 | trinotate/r2013-11-10 | None | application | computational biology | Trinotate is a comprehensive annotation suite designed for automatic functional annotation of transcriptomes, particularly de novo assembled transcriptomes, from model or non-model organisms. Trinotate makes use of a number of different well referenced methods for functional annotation including homology search to known sequence data (BLAST+/SwissProt), protein domain identification (HMMER/PFAM), protein signal peptide and transmembrane domain prediction (signalP/tmHMM), and leveraging various annotation databases (eggNOG/GO/Kegg databases). All functional annotation data derived from the analysis of transcripts is integrated into a SQLite database which allows fast efficient searching for terms with specific qualities related to a desired scientific hypothesis or a means to create a whole annotation report for a transcriptome. |
trycycler | 0.5.5 | trycycler/0.5 | None | application | bioinformatics | A tool for generating consensus long-read assemblies for bacterial genomes |
twincons | 0.6.2.dev0 | twincons/0.6 | None | application | Biology | This projects provides several packages for analysis of MSAs comprised of two sequence groups. |
twobittofa | 1.0 | twobittofa/1.0 | None | unknown | unknown | This is a bioinformatics, freely downloadable command-line software (linux.x86_64) provided by the UCSC |
ucsc-bedgraphtobigwig | 455 | ucsc-bedgraphtobigwig/455 | None | application | computational biology | Convert a bedGraph file to bigWig format. |
ucsc-bigwigaverageoverbed | 377 | ucsc-bigwigaverageoverbed/377 | None | application | computational biology | Compute average score of big wig over each bed, which may have introns. |
ucsc-fatotwobit | 377 | ucsc-fatotwobit/377 | None | application | computational biology | Convert DNA from fasta to 2bit format |
ucsc-liftover | 366 | ucsc-liftover/366 | None | application | computational biology | The Batch Coordinate Conversion (liftOver) utility converts genome coordinates and genome annotation files between assemblies. |
ucsc-twobittofa | 357 | ucsc-twobittofa/357 | None | application | computational biology | Convert all or part of .2bit file to fasta |
ucsc-twobittofa | 377 | ucsc-twobittofa/377 | None | application | computational biology | Convert all or part of .2bit file to fasta |
udunits2 | 2.2.26 | udunits2/2.2 | compiler/pgi/20 compiler/intel/20 | library | runtime support | |
ufcg | 1.0.6 | ufcg/1.0 | None | application | computational biology | UFCG pipeline provides methods for a genome-wide taxonomic profiling and annotation of your own biological sequences of Fungi. |
ultraplex | 1.2.9 | ultraplex/1.2 | None | application | computational biology | fastq demultiplexer |
umap-learn | 0.2.4 | umap-learn/py36/0.2 | None | application | learning algorithm | Uniform Manifold Approximation and Projection |
umap-learn | 0.3.10 | umap-learn/py37/0.3 | None | application | learning algorithm | Uniform Manifold Approximation and Projection |
umi_tools | 1.0.1 | umi_tools/1.0 | None | application | Bioinformatics | Tools for dealing with Unique Molecular Identifiers (UMIs) / Random Molecular Tags (RMTs) |
unicycler | 0.4.8 | unicycler/0.4 | None | application | bioinformatics | Hybrid assembly pipeline for bacterial genomes |
unicycler | 0.5.0 | unicycler/0.5 | None | application | bioinformatics | Hybrid assembly pipeline for bacterial genomes |
unikmer | 0.18.7 | unikmer/0.18 | None | application | Biology | unikmer: toolkit for nucleic acid k-mer analysis, including set operations on k-mers (sketch) optional with TaxIDs but without count information. |
uropa | 4.0.2 | uropa/4.0 | None | application | Biology | UROPA (Universal RObust Peak Annotator) is a command line based tool, intended for genomic region annotation from e.g. peak calling. It detects the most appropriate annotation by taking parameters such as feature type, anchor, direction and strand into account. Furthermore, it allows filtering for GTF attribute values, e.g. protein_coding. |
usearch | 10.0.240 | usearch/10.0 | None | application | computational biology | USEARCH is a unique sequence analysis tool with thousands of users world-wide. |
usearch | 11.0.667 | usearch/11.0 | None | application | computational biology | USEARCH is a unique sequence analysis tool with thousands of users world-wide. |
usearch | 5.2 | usearch/5.2 | None | application | computational biology | USEARCH is a unique sequence analysis tool with thousands of users world-wide. |
usearch | 6.1 | usearch/6.1 | None | application | computational biology | USEARCH is a unique sequence analysis tool with thousands of users world-wide. |
usearch | 7.0 | usearch/7.0 | None | application | computational biology | USEARCH is a unique sequence analysis tool with thousands of users world-wide. |
varscan | 2.3 | varscan/2.3 | None | application | computational biology | Variant calling and somatic mutation/CNV detection for next-generation sequencing data |
varscan | 2.4.4 | varscan/2.4 | None | application | computational biology | Variant calling and somatic mutation/CNV detection for next-generation sequencing data |
vasp | 5.4.4 | vasp/5.4 | compiler/intel/20:openmpi/4.1 | library | runtime support | |
vasp | 6.2.1 | vasp/6.2 | compiler/intel/19:openmpi/4.1 | library | runtime support | |
vasp | 6.2.1vtst | vasp/6.2vtst | compiler/intel/19:openmpi/4.1 | library | runtime support | |
vasp | 6.3.1 | vasp/6.3sol | compiler/intel/20:openmpi/4.1 | library | runtime support | |
vasp | 6.3.1 | vasp/6.3vtst | compiler/intel/20:openmpi/4.1 | library | runtime support | |
vasp | 6.3.1 | vasp/6.3 | compiler/intel/20:openmpi/4.1 | library | runtime support | |
vasp | 6.4.1 | vasp/6.4sol | compiler/intel/20:openmpi/4.1 | library | runtime support | |
vasp | 6.4.1 | vasp/6.4vtst | compiler/intel/20:openmpi/4.1 | library | runtime support | |
vasp | 6.4.3 | vasp/6.4 | compiler/intel/20:openmpi/4.1 | library | runtime support | |
vasp-acc | 6.2.1 | vasp-acc/6.2 | compiler/intel/19 | library | runtime support | |
vasp-acc | 6.3.1 | vasp-acc/6.3 | compiler/nvhpc/21.9:openmpi/3.1 compiler/intel/19 | library | runtime support | |
vasp-acc | 6.4.1 | vasp-acc/6.4 | compiler/nvhpc/21.9:openmpi/3.1 | library | runtime support | |
vaspkit | 1.5.1 | vaspkit/1.5 | None | application | Chemistry | Perform high throughput analysis from data generated by VASP. |
vcf-kit | 0.1.6 | vcf-kit/0.1 | None | application | Utilities | Assorted utilities for the variant call format |
vcf2maf | 1.6.18 | vcf2maf/1.6 | None | application | computational biology | Convert a VCF into a MAF where each variant is annotated to only one of all possible gene isoforms |
vcflib | 1.0.2 | vcflib/1.0 | None | application | Utilities | Command-line tools for manipulating VCF files |
vcftools | 0.1.16 | vcftools/0.1 | None | application | computational biology | A set of tools written in Perl and C++ for working with VCF files. |
vcontact2 | 0.9.19 | vcontact2/0.9 | None | application | Virology | Viral Contig Automatic Clustering and Taxonomy |
velvet | 1.2.10 | velvet/1.2 | None | application | computational biology | Velvet - Sequence assembler for very short reads |
velvetoptimiser | 2.2.6 | velvetoptimiser/2.2 | None | application | computational biology | Automatically optimise three of Velvet's assembly parameters. |
verifybamid2 | 2.0.1 | verifybamid2/2.0 | None | application | DNA sequencing | A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method. |
verkko | 2.0 | verkko/2.0 | None | application | computational biology | Assembler for hybrid combinations of long reads |
vesta | 3.5.8 | vesta/3.5 | None | application | visualization | VESTA is a 3D visualization program for structural models, volumetric data such as electron/nuclear densities, and crystal morphologies. |
vflp | 2020.04.19 | vflp/2020.04.19 | None | application | computational chemistry | VFLP is VirtualFlow for Ligand Preparation |
vftools | 0.0.2020.05.17 | vftools/2020.05.17 | None | application | computational chemistry | VFTools is a a loose collection of additional tools and scripts which can be useful when using VirtualFlow. |
vfvs | 2020.04.23 | vfvs/2020.04.23 | None | application | computational chemistry | VFVS is VirtualFlow for Ligand Screenings |
vfvs | 2022.07.21 | vfvs/2022.07.21 | None | application | computational chemistry | VFVS is VirtualFlow for Ligand Screenings |
vgas | 0.0.2020.07.22 | vgas/2020.07.22 | None | application | genomics | VGAS (viral genome annotation system) is a system combing ab initio method and similarity-based method, which can perform the functions of virus gene finding and function annotating merely depending on the gene sequence itself. |
vibrant | 1.0.1 | vibrant/1.0 | None | application | computational biology | Virus Identification By iteRative ANnoTation |
vibrant | 1.2.1 | vibrant/1.2 | None | application | computational biology | Virus Identification By iteRative ANnoTation |
viennarna | 2.3.3 | viennarna/2.3 | None | application | computational biology | The ViennaRNA Package consists of a C code library and several stand-alone programs for the prediction and comparison of RNA secondary structures. |
vigor4 | 0.0.2020.07.02 | vigor4/2020.07.02 | None | application | bioinformatics | VIGOR4 (Viral Genome ORF Reader) is a Java application to predict protein sequences encoded in viral genomes. |
vim | 8.1.0960 | vim/8.1 | None | application | Utility | Vim is a greatly improved version of the good old UNIX editor Vi |
viral_consensus | 0.0.5 | viral_consensus/0.0.5 | None | application | bioinformatics | Fast viral consensus genome reconstruction |
virema | 0.6 | virema/0.6 | None | application | computational biology | ViReMa (Viral Recombination Mapper) detects and reports recombination or fusion events in virus genomes using deep sequencing datasets. |
virhostmatcher | 1.0.0 | virhostmatcher/1.0 | None | application | computational biology | VirHostMatcher, matching hosts of viruses based on oligonucleotide frequency (ONF) comparison. |
virhostmatcher-net | 0.0.2021.08.29 | virhostmatcher-net/2021.08.29 | None | application | computational biology | VirHostMatcher-Net: A network-based computational tool for predicting virus-host interactions. |
virsorter | 1.0.6 | virsorter/1.0 | None | application | unknown | VirSorter2 -- A multi-classifier, expert-guided approach to detect diverse DNA and RNA virus genomes |
virsorter | 2.1 | virsorter/2.1 | None | application | unknown | VirSorter2 -- A multi-classifier, expert-guided approach to detect diverse DNA and RNA virus genomes |
visit | 2.10.2 | visit/2.10 | None | application | utility | VisIt is an Open Source, interactive, scalable, visualization, animation and analysis tool. |
vistasoft | 0fa6c4a | vistasoft/0fa6c4a | None | application | matlab toolbox | VISTASOFT contains Matlab code to perform a variety of analysis on MRI data, including functional MRI and diffusion MRI. |
vmd | 1.9.3 | vmd/1.9 | None | application | molecular dynamics | VMD is designed for modeling, visualization, and analysis of biological systems such as proteins, nucleic acids, lipid bilayer assemblies, etc. It may be used to view more general molecules, as VMD can read standard Protein Data Bank (PDB) files and display the contained structure. VMD provides a wide variety of methods for rendering and coloring a molecule: simple points and lines, CPK spheres and cylinders, licorice bonds, backbone tubes and ribbons, cartoon drawings, and others. VMD can be used to animate and analyze the trajectory of a molecular dynamics (MD) simulation. In particular, VMD can act as a graphical front end for an external MD program by displaying and animating a molecule undergoing simulation on a remote computer. |
vrhyme | 1.1.0 | vrhyme/1.1 | None | application | bioinformatics | vRhyme functions by utilizing coverage variance comparisons and supervised machine learning classification of sequence features to construct viral metagenome-assembled genomes (vMAGs). |
vs-code | 1.90.2 | vs-code/1.90 | None | application | Development | Visual Studio Code |
vs-code-cli | 1.90.2 | vs-code-cli/1.90 | None | application | Development | Visual Studio Code |
vsearch | 2.10.0 | vsearch/2.10 | None | application | computational biology | A versatile open source tool for metagenomics (USEARCH alternative) |
vsearch | 2.18.0 | vsearch/2.18 | None | application | computational biology | A versatile open source tool for metagenomics (USEARCH alternative) |
wannier90 | 3.1 | wannier90/3.1 | compiler/intel/20:openmpi/4.0 compiler/intel/19:openmpi/4.1 compiler/gcc/9:openmpi/4.0 compiler/intel/19:openmpi/4.0 compiler/gcc/10:openmpi/4.1 compiler/gcc/10:openmpi/4.0 compiler/gcc/11:openmpi/4.1 compiler/intel/20:openmpi/4.1 | library | runtime support | |
wannierberri | 0.11.1 | wannierberri/py38/0.11 | None | application | physics | Advanced tool for Wannier interpolation and integration of k-space integrals |
wannierberri | 0.11.1 | wannierberri/py39/0.11 | None | application | physics | Advanced tool for Wannier interpolation and integration of k-space integrals |
wanniertools | 2.7.0 | wanniertools/2.7 | compiler/intel/20:openmpi/4.1 | application | chemistry | |
weblogo | 3.7.4 | weblogo/3.7 | None | application | Utility | WebLogo3 : Sequence Logos Redrawn |
wevote | 1.8 | wevote/1.8 | None | library | runtime support | |
wgddetector | 1.1 | wgddetector/1.1 | None | application | Biology | WGDdetector: a pipeline for whole genome duplication (WGD) detecting with the genome or transcriptome annotations. |
wgrib | 1.8 | wgrib/1.8 | compiler/pgi/20 compiler/intel/20 | application | file processing | WGRIB is a program to manipulate, inventory and decode GRIB files. |
wgrib2 | 2.0.6 | wgrib2/2.0 | None | application | file processing | wgrib2 is more like four drawers of kitchen utensils as well as the microwave and blender. |
wtdbg | 2.5 | wtdbg/2.5 | None | application | Bioinformatics | Wtdbg2: A fuzzy Bruijn graph approach to long noisy reads assembly |
xcrysden | 1.5.60 | xcrysden/1.5 | None | application | physics | XCrySDen is a crystalline and molecular structure visualisation program aiming at display of isosurfaces and contours, which can be superimposed on crystalline structures and interactively rotated and manipulated. |
xcrysden | 1.6.2 | xcrysden/1.6 | None | application | physics | XCrySDen is a crystalline and molecular structure visualisation program aiming at display of isosurfaces and contours, which can be superimposed on crystalline structures and interactively rotated and manipulated. |
xpclr | 1.1.2 | xpclr/1.1 | None | application | Bioinformatics | Code to compute xp-clr values to detect selection as per Chen, Patterson & Reich 2010. |
xzutils | 5.2 | xzutils/5.2 | compiler/intel/19 compiler/intel/18 compiler/gcc/11 compiler/intel/20 None compiler/gcc/9 compiler/gcc/10 compiler/pgi/20 | library | runtime support | |
yambo | 5.2.3 | yambo/5.2 | compiler/gcc/11:openmpi/4.1 | application | realistic materials | Open-source many-body perturbation theory and time-dependent density functional theory |
yaml-cpp | 0.7 | yaml-cpp/0.7 | compiler/intel/20 compiler/gcc/10 | library | runtime support | |
zerone | 1.0 | zerone/1.0 | None | application | computational biology | Zerone discretizes several ChIP-seq replicates simultaneously and resolves conflicts between them. After the job is done, Zerone checks the results and tells you whether it passes the quality control. |
zlib | 1.2 | zlib/1.2 | compiler/gcc/9 None compiler/gcc/11 compiler/intel/19 compiler/pgi/20 compiler/intel/2021 compiler/intel/20 compiler/intel/18 compiler/gcc/10 | library | runtime support | |
zorro | 2011.12.01 | zorro/2011.12.01 | None | application | bioinformatics | ZORRO is a probabilistic masking program that assigns confidence scores to each column in a multiple sequence alignment. |