cnvkit binary package in Ubuntu Lunar amd64

 A command-line toolkit and Python library for detecting copy number variants
 and alterations genome-wide from targeted DNA sequencing. It is designed for
 use with hybrid capture, including both whole-exome and custom target panels,
 and short-read sequencing platforms such as Illumina and Ion Torrent.

Publishing history

Date Status Target Pocket Component Section Priority Phased updates Version
  2022-10-27 17:20:10 UTC Published Ubuntu Lunar amd64 release universe science Optional 0.9.9-2
  • Published
  • Copied from ubuntu jammy-proposed amd64 in Primary Archive for Ubuntu

Source package