SnifflesStructural variation caller using third generation sequencing
Hap.pyHaplotype VCF comparison tools
Dash.jlDash for Julia - A Julia interface to the Dash ecosystem for creating analytic web applications in Julia. No JavaScript required.
BiopythonOfficial git repository for Biopython (originally converted from CVS)
Cyvcf2cython + htslib == fast VCF and BCF processing
StrelkaStrelka2 germline and somatic small variant caller
SourmashQuickly search, compare, and analyze genomic and metagenomic data sets.
Homebrew Bio🍺🔬 Bioinformatics formulae for the Homebrew package manager (macOS and Linux)
Hh SuiteRemote protein homology detection suite.
DashAnalytical Web Apps for Python, R, Julia, and Jupyter. No JavaScript Required.
BowtieAn ultrafast memory-efficient short read aligner
Abyss🔬 Assemble large genomes using short reads
MiniasmUltrafast de novo assembly for long noisy reads (though having no consensus step)
Bedops🔬 BEDOPS: high-performance genomic feature operations
MinigraphProof-of-concept seq-to-graph mapper and graph generator
Allensdkcode for reading and processing Allen Institute for Brain Science data
SequenceserverIntuitive local web frontend for the BLAST bioinformatics tool
IntermineA powerful open source data warehouse system
Dgl LifesciPython package for graph neural networks in chemistry and biology
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Raxml NgRAxML Next Generation: faster, easier-to-use and more flexible
Seqan3The modern C++ library for sequence analysis. Contains version 3 of the library and API docs.
KaryoploterkaryoploteR - An R/Bioconductor package to plot arbitrary data along the genome
RibbonA genome browser that shows long reads and complex variants better
Janggu Deep learning infrastructure for bioinformatics
SurvivorToolset for SV simulation, comparison and filtering
Deep RulesTen Quick Tips for Deep Learning in Biology
QuastGenome assembly evaluation tool
RoaryRapid large-scale prokaryote pan genome analysis
CuneiformCuneiform distributed programming language
Goleftgoleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
AfterqcAutomatic Filtering, Trimming, Error Removing and Quality Control for fastq data
FgbioTools for working with genomic and high throughput sequencing data.
BiosyntaxSyntax highlighting for computational biology
RagooFast Reference-Guided Scaffolding of Genome Assembly Contigs. RagTag, the successor to RaGOO, is now available here: https://github.com/malonge/RagTag
SnprThe sources of the openSNP website
ClairvoyanteClairvoyante: a multi-task convolutional deep neural network for variant calling in Single Molecule Sequencing
Soapdenovo2Next generation sequencing reads de novo assembler.
MixcrMiXCR is a universal software for fast and accurate extraction of T- and B- cell receptor repertoires from any type of sequencing data. Free for academic use only.
ScdeR package for analyzing single-cell RNA-seq data
KaijuFast taxonomic classification of metagenomic sequencing reads using a protein reference database
PysradbPackage for fetching metadata and downloading data from SRA/ENA/GEO