| ad2vcf | | Add allelic depth info from a SAM stream to a VCF file |
| arka | | Graphic interface for the programs from the GP package |
| atac-seq | | Core tools needed for ATAC-Seq analysis |
| azara | | Programs to process and view NMR data |
| balance-tui | | Balance chemical equations from the CLI |
| bcf-score | | Bcftools plugin for mosaic chromosomal alteration analysis |
| bcftools | | Tools for manipulating BCF and VCF variant call files |
| beagle | | Phasing genotypes and imputing ungenotyped markers |
| bedtools | | Swiss army knife for genome arithmetic |
| bio-mocha | | Bcftools plugin for mosaic chromosomal alteration analysis |
| biolibc | | Low-level high-performance bioinformatics library |
| biolibc-tools | | High-performance bioinformatics tools based on biolibc |
| bioperl | | Perl tools for computational molecular biology |
| bioruby (V) | | Intergrated environment for Bioinformatics using Ruby |
| biostar-tools (V) | | Meta-package for Biostar Handbook tools |
| bodr | | Blue Obelisk Data Repository |
| bowtie2 | | Ultrafast, memory-efficient short read aligner |
| bwa | | Map low-divergent sequences against a large reference genome |
| canu | | Single molecule sequence assembler for genomes large and small |
| cdhit | | Clustering and comparing protein or nucleotide sequences |
| chemtool | | Program for drawing organic molecules |
| chip-seq | | Core tools needed for ChIP-Seq analysis |
| clustalw | | General purpose multiple alignment program for DNA or proteins |
| coalesce | | Estimates effective population size and mutation rate |
| coordgenlibs | | 2D coordinate generation for molecules |
| fasda | | Fast and simple differential analysis |
| fastDNAml | | Program derived from Joseph Felsenstein's version 3.3 DNAML |
| fastp | | Ultra-fast all-in-one FASTQ preprocessor |
| fastq-trim | | Lightening fast sequence read trimmer |
| fastqc | | Quality control tool for high throughput sequence data |
| fasttree | | Approximately-maximum-likelihood phylogenetic trees from alignments |
| fastx-toolkit | | CLI tools for Short-Reads FASTA/FASTQ files preprocessing |
| filter-fastq | | Filter reads from a FASTQ file |
| fluctuate | | Estimation of population growth rate |
| gabedit | | Graphical User Interface to computational chemistry packages |
| generand | | Generate random genomic data in FASTA/FASTQ, SAM, or VCF format |
| genesplicer | | Computational Method for Splice Site Prediction |
| gffread | | GFF/GTF format conversions, filtering, FASTA extraction, etc |
| glimmer | | System for finding genes in microbial DNA |
| gp | | Manipulate DNA/RNA sequence in a Unix fashion |
| gromacs | | Molecular dynamics package |
| haplohseq | | Identify regions of allelic imbalance |
| hisat2 | | Alignment program for mapping next-generation sequencing reads |
| hmmer | | Implementation of profile HMM software for protein sequence analysis |
| htslib | | C library for high-throughput sequencing data formats |
| igv | | Visualization tool for genomic datasets |
| jmol (V) | | Jmol: an open-source Java viewer for chemical structures in 3D |
| kallisto | | Quantify abundances of transcripts from RNA-Seq data |
| libpll | | High-performance software library for phylogenetic analysis |
| lucy | | Sequence Cleanup Program |
| maeparser | | Parser for Maestro file format |
| mca-calling | | Core tools for Mosaic Chromosomal Alteration event calling |
| microsynteny-tools | | Tools for exploring microsyntenic differences among species |
| miniasm | | OLC-based de novo assembler for long reads |
| minimap2 | | Sequence alignment program for noisy, long reads |
| mmdb (V) | | Macromolecular coordinate library |
| molsketch | | Program for drawing molecular structures |
| mopac | | Semi-empirical (MNDO, etc.) molecular orbital calculation |
| mpqc | | The Massively Parallel Quantum Chemistry Program |
| mummer | | System for aligning whole genome sequences |
| nanocomp (V) | | Compare runs of Oxford Nanopore sequencing data and alignments |
| nanofilt (V) | | Filtering and trimming of Oxford Nanopore sequencing data |
| nanoget (V) | | Extract information from Oxford Nanopore sequencing data |
| nanolyse (V) | | Removing reads mapping to the lambda genome |
| nanomath (V) | | Math functions for other Oxford Nanopore processing scripts |
| nanoplot (V) | | Plotting suite for Oxford Nanopore sequencing data and alignments |
| nanoQC (V) | | Create fastQC-like plots for Oxford Nanopore sequencing data |
| nanostat (V) | | Statistics for Oxford Nanopore sequencing data and alignments |
| ncbi-blast+ | | NCBI implementation of Basic Local Alignment Search Tool |
| nutsqlite | | Record what you eat and analyze your meals |
| openbabel | | Chemistry file translation program |
| p5-Bio-ASN1-EntrezGene | | Regular expression-based Perl Parser for NCBI Entrez Gene |
| pdbalign | | Prediction of Protein Secondary Structure and Active Sites |
| peak-classifier | | Classify ChIP/ATAC-Seq peaks based on features provided in a GFF |
| phylip | | Phylogeny Inference Package |
| plink | | Whole-genome association analysis toolset |
| plinkseq | | C/C++ library for working with human genetic variation data |
| primer3 | | Design PCR primers |
| profit | | Performs least squares fits of two protein structures |
| puzzle | | Maximum likelihood analysis of molecular sequence data |
| py-ase (V) | | Atomic Simulation Environment |
| py-bcbio-gff | | Read and write Generic Feature Format (GFF) with Biopython integration |
| py-biofrills (V) | | Bioinformatics utilities for molecular sequence analysis |
| py-biopython | | Python libraries for computational molecular biology |
| py-cantera (V) | | Chemical kinetics, thermodynamics, and transport tool suite |
| py-cclib (V) | | Parsers and algorithms for computational chemistry |
| py-chemicals (V) | | Chemical properties component of ChEDL library |
| py-chempy (V) | | Python package useful for solving problems in chemistry |
| py-cobrapy (V) | | Package for constraints-based modeling of biological networks |
| py-cogent (V) | | Cogent A toolkit for statistical analysis of biological sequences |
| py-csb (V) | | Computational Structural Biology Toolbox |
| py-cutadapt | | Find and remove adapter sequences, primers, poly-A tails, etc |
| py-deap (V) | | Distributed Evolutionary Algorithms in Python |
| py-dna-features-viewer | | Python library to visualize DNA features, e.g. GenBank or Gff files |
| py-dnaio | | Read and write FASTQ and FASTA files |
| py-geppy (V) | | Package for gene expression programming in Python |
| py-gnm (V) | | Python Gaussian Network Model |
| py-gpaw (V) | | Grid-based real-space PAW method DFT code |
| py-htseq (V) | | Python library to facilitate programmatic analysis of sequence data |
| py-macs2 | | Algorithm for identifying transcription factor binding sites |