Annoate a .vcf file with publicly-available data

Structural and functional analysis of DIDA variants

Conan package for https://github.com/martinmoene/variant-lite

HGVS variant name parsing and generation

REST Interface for VariantValidator. Includes docker container

Accurate matching of variant alleles using local haplotypes

Covid-19 Mu Variant [B.1.621] Prediction and Classification Artificial Intelligence/Machine Learning Software

GATK variant calling for RNASeq

A snakemake pipeline that performs variant calling of Nanopore reads from FastQ files for non-model organisms

Mirror of tryton product module

Automated ACMG/AMP classification for human variants associated with congenital hearing loss

A Loop-Mediated Isothermal Amplification (LAMP) concatemer analysis, variant calling, and polishing tool

Var3PPred: Variant prediction based on 3-D structure and sequence analyses of protein-protein interactions on Autoinflammatory Disease

Implements pieces from various shogi variants (standard, Wa, Tori, Okisaki) on an arbitrary board size

Lightweight and memory efficient reader for PLINK BED files. It supports both SNP-major and individual-major formats. Written in pure Python.

HGVS variant description parser

Tool suite for HGVS variant descriptions