ExomeDepth (1.1.10)

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Calls Copy Number Variants from Targeted Sequence Data.

http://cran.r-project.org/web/packages/ExomeDepth

Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.

Maintainer: Vincent Plagnol
Author(s): Vincent Plagnol

License: GPL-3

Uses: aod, VGAM, knitr

Released 10 months ago.


6 previous versions

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