Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
Version: | 1.1.10 |
Depends: | R (≥ 3.3.0) |
Imports: | Biostrings, IRanges, Rsamtools, GenomicRanges (≥ 1.23.0), aod, VGAM (≥ 0.8.4), methods, GenomicAlignments |
Suggests: | knitr |
Published: | 2016-05-15 |
Author: | Vincent Plagnol |
Maintainer: | Vincent Plagnol <v.plagnol at ucl.ac.uk> |
License: | GPL-3 |
NeedsCompilation: | yes |
CRAN checks: | ExomeDepth results |
Reference manual: | ExomeDepth.pdf |
Vignettes: |
ExomeDepth |
Package source: | ExomeDepth_1.1.10.tar.gz |
Windows binaries: | r-devel: ExomeDepth_1.1.10.zip, r-release: ExomeDepth_1.1.10.zip, r-oldrel: ExomeDepth_1.1.10.zip |
OS X El Capitan binaries: | r-release: not available |
OS X Mavericks binaries: | r-oldrel: ExomeDepth_1.1.10.tgz |
Old sources: | ExomeDepth archive |
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