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[ Source: cnvkit  ]

Paketti: cnvkit (0.9.8-1)

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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.

Muut pakettiin cnvkit liittyvät paketit

  • depends
  • recommends
  • suggests
  • enhances

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Imurointi kaikille saataville arkkitehtuureille
Arkkitehtuuri Paketin koko Koko asennettuna Tiedostot
amd64 15,065.2 kt69,059.0 kt [tiedostoluettelo]
arm64 15,065.2 kt69,059.0 kt [tiedostoluettelo]
ppc64el 15,065.2 kt69,059.0 kt [tiedostoluettelo]