Stars
Annotate models of genetic inheritance patterns in variant files (vcf files)
A nextflow pipeline to run Fluffy
Clinical-Genomics / raredisease
Forked from nf-core/rarediseaseCG's rare disease pipeline in next flow, see the main repo here 👇
Collection of tools that are used in the facilities
nim wrapper for htslib for parsing genomics data files
lh3 / htsbox
Forked from samtools/htslibMy experimental tools on top of htslib. NOT OFFICIAL!!!
High-performance error correction for Illumina resequencing data
RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference transposable elements. Please read the wiki page (link belo…
Gene lists and some elementary tools for handling them.
This repository contains data indexes from NIST's Genome in a Bottle project.