ExomeCNV (1.2)
Detect CNV and LOH from Exome Sequecing Data.
http://cran.r-project.org/web/packages/ExomeCNV
ExomeCNV is a statistical method to detect CNV and LOH using depth-of-coverage and B-allele frequencies from mapped short sequence reads in exome sequencing data.
Maintainer:
J. Fah Sathirapongsasuti
Author(s): J. Fah Sathirapongsasuti, Hane Lee, and Stanley F. Nelson
License: LGPL-2.1
Uses: Does not use any package
Released over 1 year ago.
