R scripts for plotting and assessing XHMM whole-exome-sequencing-based CNV calls. XHMM (eXome Hidden Markov Model) is a C++ software package (http://atgu.mgh.harvard.edu/xhmm) written to call copy number variation (CNV) from next-generation sequencing projects, where exome capture was used (or targeted sequencing, more generally). This R package enables the user to visualize both the PCA normalization performed by XHMM and the CNVs it has called.
Version: | 1.1 |
Depends: | R (≥ 2.14.0) |
Imports: | gplots, plotrix |
Published: | 2014-06-15 |
Author: | Menachem Fromer |
Maintainer: | Menachem Fromer <fromer at broadinstitute.org> |
BugReports: | http://groups.google.com/a/broadinstitute.org/group/xhmm-users |
License: | GPL-2 |
URL: | http://atgu.mgh.harvard.edu/xhmm |
NeedsCompilation: | no |
CRAN checks: | xhmmScripts results |
Reference manual: | xhmmScripts.pdf |
Package source: | xhmmScripts_1.1.tar.gz |
Windows binaries: | r-devel: xhmmScripts_1.1.zip, r-release: xhmmScripts_1.1.zip, r-oldrel: xhmmScripts_1.1.zip |
OS X Snow Leopard binaries: | r-release: xhmmScripts_1.1.tgz, r-oldrel: xhmmScripts_1.1.tgz |
OS X Mavericks binaries: | r-release: xhmmScripts_1.1.tgz |
Old sources: | xhmmScripts archive |