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ExomeDepth (version 1.1.5)

Calls Copy Number Variants from Targeted Sequence Data

Description

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

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Install

install.packages('ExomeDepth')

Monthly Downloads

105

Version

1.1.5

License

GPL-3

Maintainer

Last Published

May 29th, 2015

Functions in ExomeDepth (1.1.5)