an implementation of the inference pipeline of AlphaFold v2.0 using a completely new model that was entered in CASP14.

A long-read analysis toolbox for cancer genomics.

a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed.

a cross-platform ultrafast comprehensive toolkit for FASTA/Q processing.

structural variant calling and genotyping with existing tools, but, smoothly.

Accurate prediction of protein structures and interactions using a 3-track network

(Sequence Alignment/Map) a generic format for storing large nucleotide sequence alignments that provides various utilities for manipulating alignments, including sorting, merging, indexing and generating alignments in a per-position format.