UnleashUnleash is the open source feature toggle service.
civic-clientWeb client for CIViC: Clinical Interpretations of Variants in Cancer
witty.erWhat is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.
MTBseq sourceMTBseq is an automated pipeline for mapping, variant calling and detection of resistance mediating and phylogenetic variants from illumina whole genome sequence data of Mycobacterium tuberculosis complex isolates.
TeamTeriGenomics using open source tools, running on GCP or AWS
g3vizLollipop-diagram to interactively visualize genetic mutations
pathoscorepathoscore evaluates variant pathogenicity tools and scores.
variantkeyNumerical Encoding for Human Genetic Variants
spark-vcfSpark VCF data source implementation for Dataframes
ordoOrdo: A minimalist language with row polymorphism
phenomenet-vpA phenotype-based tool for variant prioritization in WES and WGS data
vcf stuff📊Evaluating, filtering, comparing, and visualising VCF
CuteVCFsimple viewer for variant call format using htslib
pepperPEPPER-Margin-DeepVariant
HarbolHarbol is a collection of data structure and miscellaneous libraries, similar in nature to C++'s Boost, STL, and GNOME's GLib
pulsar-core🚀 Handy dynamic styles utilities for React Native and React Native Web.
rvtestsRare variant test software for next generation sequencing data
styled-variantsA scalable styled-component theming system that fully leverages JavaScript as a language for styles authoring and theming at both local and global levels.
HLAxHLA: Fast and accurate HLA typing from short read sequence data
indigoIndigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products