Detect CNV and LOH from Exome Sequecing Data 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. Software Depends: DNAcopy J. Fah Sathirapongsasuti <fsathira@fas.harvard.edu> J. Fah Sathirapongsasuti, Hane Lee, and Stanley F. Nelson LGPL-2.1 2011-10-28 application/tgz http://CRAN.R-project.org/package=ExomeCNV