[ Pakiet źródłowy: cnvkit ]
Pakiet: cnvkit (0.9.5-3)
Odnośniki dla cnvkit
Zasoby systemu Debian:
- Raporty o błędach
- Developer Information
- Dziennik zmian w systemie Debian
- Informacje nt. praw autorskich
- Śledzenie łatek systemu Debian
Pobieranie pakietu źródłowego cnvkit:
Opiekunowie:
- Debian Med Packaging Team (Strona QA, Archiwum e-mail)
- Michael R. Crusoe (Strona QA)
- Steffen Moeller (Strona QA)
- Olivier Sallou (Strona QA)
Zasoby zewnętrzne:
- Strona internetowa [cnvkit.readthedocs.org]
Podobne pakiety:
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.
Inne pakiety związane z cnvkit
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- dep: python3-scipy
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- dep: r-bioc-dnacopy
- R package: DNA copy number data analysis
Pobieranie cnvkit
Architektura | Rozmiar pakietu | Rozmiar po instalacji | Pliki |
---|---|---|---|
amd64 | 22 378,8 KiB | 22 874,0 KiB | [lista plików] |