cnvkit binary package in Ubuntu Mantic 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 | Component | Section | Priority | Phased updates | Version | ||
|---|---|---|---|---|---|---|---|---|---|
| 2023-04-25 12:10:09 UTC | Published | Ubuntu Mantic amd64 | release | universe | science | Optional | 0.9.9-2 | ||
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