[ Source: cnvkit ]
Package: cnvkit (0.9.8-1)
Links for cnvkit
Debian Resources:
Download Source Package cnvkit:
Maintainers:
- Debian Med Packaging Team (QA Page, Mail Archive)
- Michael R. Crusoe (QA Page)
- Steffen Moeller (QA Page)
- Olivier Sallou (QA Page)
External Resources:
- Homepage [cnvkit.readthedocs.org]
Similar packages:
Copy number variant detection from targeted DNA sequencing
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.
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Download cnvkit
| Architecture | Package Size | Installed Size | Files |
|---|---|---|---|
| amd64 | 15,065.2 kB | 69,059.0 kB | [list of files] |
| arm64 | 15,065.2 kB | 69,059.0 kB | [list of files] |
| ppc64el | 15,065.2 kB | 69,059.0 kB | [list of files] |