Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
Info: This package contains files in non-standard
labels.
linux-64
v1.1.16
osx-64
v1.1.16
conda install
To install this package run one of the following: conda install bioconda::r-exomedepthconda install bioconda/label/cf201901::r-exomedepthconda install bioconda/label/gcc7::r-exomedepth
