Stampy — Wellcome Centre for Human Genetics

Stampy — Wellcome Centre for Human Genetics

Stampy is a package for the mapping of short reads from illumina sequencing machines onto a refer...概要を表示 Stampy is a package for the mapping of short reads from illumina sequencing machines onto a reference genome. It's recommended for most workflows, including those for genomic resequencing, RNA-Seq and Chip-seq. Stampy excels in the mapping of reads containing that contain sequence variation relative to the reference, in particular for those containing insertions or deletions. It can map reads from

• NGS