Calls CNV from exome sequence data Calls copy number variants (CNVs) from targeted sequence data Software Depends: R (>= 2.14.0), methods, aod, VGAM (>= 0.8.4), GenomicRanges (>= 1.6.7), Rsamtools Imports: methods, aod, VGAM, GenomicRanges, Rsamtools Vincent Plagnol <v.plagnol@ucl.ac.uk> Vincent Plagnol GPL-3 2012-04-28 application/tgz http://CRAN.R-project.org/package=ExomeDepth