ExomeDepth: Calls Copy Number Variants from Targeted Sequence Data
Version 1.1.10

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

Package details

AuthorVincent Plagnol
Date of publication2016-05-15 09:48:08
MaintainerVincent Plagnol <[email protected]>
LicenseGPL-3
Version1.1.10
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("ExomeDepth")

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ExomeDepth documentation built on May 29, 2017, 12:32 p.m.