🐟 🍣 🍱 Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using selective alignment

C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings

Signal-level algorithms for MinION data

A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.

Transcript assembly and quantification for RNA-Seq

Genome-wide Efficient Mixed Model Association

Program for analysing NGS data.

Software for clustering de novo assembled transcripts and counting overlapping reads

A package for population structure inference from RAD-seq data

genotyping microhaplotypes