Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
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Vincent Plagnol, 2 years ago
Browse source code at
Vincent Plagnol [aut, cre]
Imports Biostrings, IRanges, Rsamtools, GenomicRanges, aod, VGAM, methods, GenomicAlignments, dplyr, magrittr
See at CRAN