ad2vcf | | Add allelic depth info from a SAM stream to a VCF file |
arka | | Graphic interface for the programs from the GP package |
azara | | Programs to process and view NMR data |
bcftools | | Tools for manipulating BCF and VCF variant call files |
beagle | | Phasing genotypes and imputing ungenotyped markers |
bedtools | | Swiss army knife for genome arithmetic |
biolibc | | Low-level high-performance bioinformatics library |
biolibc-tools | | High-performance bioinformatics tools based on biolibc |
bioperl | | Perl tools for computational molecular biology |
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 |
chemical-mime-data | | Chemical mime and file type support for desktops |
chemtool | | Program for drawing organic molecules |
clustalw | | General purpose multiple alignment program for DNA or proteins |
coalesce | | Estimates effective population size and mutation rate |
coordgenlibs | | 2D coordinate generation for molecules |
fastDNAml | | Program derived from Joseph Felsenstein's version 3.3 DNAML |
fastp | | Ultra-fast all-in-one FASTQ preprocessor |
fastqc | | Quality control tool for high throughput sequence data |
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 |
glimmer | | System for finding genes in microbial DNA |
gnome-chemistry-utils | | GChemPaint, a 2D chemical editor and other programs |
gp | | Manipulate DNA/RNA sequence in a Unix fashion |
gromacs | | Molecular dynamics package |
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 |
kallisto | | Quantify abundances of transcripts from RNA-Seq data |
lucy | | Sequence Cleanup Program |
maeparser | | Parser for Maestro file format |
miniasm | | OLC-based de novo assembler for long reads |
minimap2 | | Sequence alignment program for noisy, long reads |
molsketch | | Program for drawing molecular structures |
mopac | | Molecular energy calculation program |
mpqc | | The Massively Parallel Quantum Chemistry Program |
mummer | | System for aligning whole genome sequences |
ncbi-blast+ | | NCBI implementation of Basic Local Alignment Search Tool |
nut | | 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-biopython | | Python libraries for computational molecular biology |
py-cutadapt | | Find and remove adapter sequences, primers, poly-A tails, etc |
py-dnaio | | Read and write FASTQ and FASTA files |
py-pydicom | | Pure python package for working with DICOM files |
R-popbio | | Construction and Analysis of Matrix Population Models |
racon | | Genomic consensus builder |
rasmol | | Molecular Graphics Visualisation Tool |
samtools | | Tools for manipulating sequence alignment maps |
sewer | | SEquence Analysis using WEb Resources |
stacks | | Software pipeline for building loci from short-read sequences |
stride | | Protein secondary structure assignment from atomic coordinates |
trimmomatic | | Flexible read trimming tool for Illumina NGS data |
vcf-split | | Split a multi-sample VCF into single-sample VCFs |
vcf2hap | | Generate .hap file from VCF for haplohseq |
vsearch | | Versatile open-source tool for metagenomics |
xylem | | Tools for manipulation of genetic databases |