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

Annoate a .vcf file with publicly-available data

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

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

REST Interface for VariantValidator. Includes docker container

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

Structural and functional analysis of DIDA variants

HGVS variant name parsing and generation

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

GATK variant calling for RNASeq

Accurate matching of variant alleles using local haplotypes

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

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

HGVS variant description parser

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

Tool suite for HGVS variant descriptions

Mirror of tryton product module