Package: ExomeDepth
Type: Package
Title: Calls Copy Number Variants from Targeted Sequence Data
Version: 1.1.10
Date: 2016-05-13
Depends: R (>= 3.3.0)
Imports: Biostrings, IRanges, Rsamtools, GenomicRanges (>= 1.23.0),
        aod, VGAM (>= 0.8.4), methods, GenomicAlignments
Suggests: knitr
VignetteBuilder: knitr
Author: Vincent Plagnol
Maintainer: Vincent Plagnol  <v.plagnol@ucl.ac.uk>
Description: Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.
License: GPL-3
NeedsCompilation: yes
Packaged: 2016-05-15 02:15:29 UTC; ucbtvyp
Repository: CRAN
Date/Publication: 2016-05-15 09:48:08
Built: R 3.5.1; x86_64-conda_cos6-linux-gnu; 2018-12-27 04:34:14 UTC; unix
