A versatile pairwise aligner for genomic and spliced nucleotide sequences

A simple integer compression library in Java

An extremely fast bundler for the web

Modern CSS framework based on Flexbox

Bioinformatics I/O libraries in Rust

Variant Interpretation Pipeline

Clair3-Trio: variant calling in trio using Nanopore long-reads

Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling

Structural variation caller using third generation sequencing

Vite plugin that embeds .js and .css as base85 data

TypeScript VCF library with support for both reading and writing

A universal router for Solid inspired by Ember and React Router

A declarative, efficient, and flexible JavaScript library for building user interfaces.

annotates VCF samples with denovo and possible compound flags and matching inheritance modes

Embeddable genomic visualization component based on the Integrative Genomics Viewer

This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html

Decision tree module for the Variant Interpretation Pipeline (vip)

The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants

Report API for Variant Call Format (VCF) Report templates

Report generator for Variant Call Format (VCF) files

Report template for Variant Call Format (VCF) Report generator