Randomly subsample sequencing reads or alignments

Creating alignment plots from bam files

Utility to check Binary Sequence Alignment / Map (BAM) files for corruption and repair them

Identifies multiple SNVs within the same codon, reclassifies them as MNVs, and accurately computes resulting amino acid changes from genomic reads

AI algorithms visualization made with Rust

an API for intersections of genomic data

extract nucleotide/read counts at user specific loci from multiple bam files

htsget Rust indexer (from BAM to {CSV, JSON, DB})