r-exomedepth

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

Home https://CRAN.R-project.org/package=ExomeDepth
Versions 1.1.10
License GPL-3
Recipe https://github.com/bioconda/bioconda-recipes/tree/master/recipes/r-exomedepth

Installation

With an activated Bioconda channel (see 2. Set up channels), install with:

conda install r-exomedepth

and update with:

conda update r-exomedepth

docker

A Docker container is available at https://quay.io/repository/biocontainers/r-exomedepth.