Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men

Dissecting data structures

Bayesian haplotype-based genetic polymorphism discovery and genotyping.

A simple, lightweight PowerShell script to remove pre-installed apps, disable telemetry, as well as perform various other changes to customize, declutter and improve your Windows experience. Win11D…

Simple test framework for Nextflow pipelines

Circular visualization in Python (Circos Plot, Chord Diagram, Radar Chart)

Targeted genotyper for complex polymorphic genes

A lightweight R package for performing association meta-analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using MetaSTAARlite pipeline

An R package for performing MetaSTAAR procedure in whole-genome sequencing studies

A patch for GNU Core Utilities cp, mv to add progress bars

💥💻💥 A data-parallel functional programming language

Meta Imputation of Low Coverage Sequencing

Lossless VCF compression

A feature-rich command-line audio/video downloader

Useful resources for using the Parquet format

Code written for the long-read 1KG project

SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel

A framework for building user interfaces declaratively, with XML markup and flexible theming

Library for quickly generating interactive SVGs

Easy genomic regions for short-read variant calling

A curation of WebAssembly (Wasm) resources, projects, and communities.

This API provides programmatic access to the AlphaGenome model developed by Google DeepMind.

Scalable Nextflow implementation of germline alignment and short variant calling with Parabricks for NCI Gadi HPC.

Accelerated genomics workflows in NextFlow

Complex structural variant visualization for HiFi sequencing data

Explore genomes in the terminal. Light, blazing fast 🚀, vim-motion.