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[ Source: cnvkit  ]

Paketti: cnvkit (0.9.10-2)

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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

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  • enhances

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