Python library to parse, format, validate, normalize, and map sequence v...
Long read / genome alignment software
Randomly subsample sequencing reads
Intervene: a tool for intersection and visualization of multiple genomic...
De novo genome assembly and multisample variant calling
Generic but comprehensive pipeline for prokaryotic genome annotation and...
H.E.L.E.N. (Homopolymer Encoded Long-read Error-corrector for Nanopore)
Long-reads Gap-free Chromosome-scale Assembler
Bioinformatics on GCP, AWS or Azure