[ Källkod: cnvkit ]
Paket: cnvkit (0.9.8-1)
Länkar för cnvkit
Debianresurser:
Hämta källkodspaketet cnvkit:
Ansvariga:
- Debian Med Packaging Team (QA-sida, E-postarkiv)
- Michael R. Crusoe (QA-sida)
- Steffen Moeller (QA-sida)
- Olivier Sallou (QA-sida)
Externa resurser:
- Hemsida [cnvkit.readthedocs.org]
Liknande paket:
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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Hämta cnvkit
| Arkitektur | Paketstorlek | Installerad storlek | Filer |
|---|---|---|---|
| amd64 | 15.065,2 kbyte | 69.059,0 kbyte | [filförteckning] |