Calls copy number variants (CNVs) from targeted sequence data
| Version: | 1.0.7 |
| Depends: | R (≥ 2.15.0), methods, aod, VGAM (≥ 0.8.4), GenomicRanges (≥ 1.8.10), Rsamtools |
| Published: | 2014-07-20 |
| 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: |
Using ExomeDepth |
| Package source: | ExomeDepth_1.0.7.tar.gz |
| Windows binaries: | r-devel: ExomeDepth_1.0.7.zip, r-release: ExomeDepth_1.0.7.zip, r-oldrel: ExomeDepth_1.0.7.zip |
| OS X Snow Leopard binaries: | r-release: ExomeDepth_1.0.7.tgz, r-oldrel: ExomeDepth_1.0.7.tgz |
| OS X Mavericks binaries: | r-release: ExomeDepth_1.0.7.tgz |
| Old sources: | ExomeDepth archive |