Calls copy number variants (CNVs) from targeted sequence data
| Version: | 0.9.7 |
| Depends: | R (≥ 2.14.0), methods, aod, VGAM (≥ 0.8.4), GenomicRanges (≥ 1.6.7), Rsamtools |
| Imports: | methods, aod, VGAM, GenomicRanges, Rsamtools |
| Suggests: | GenomicRanges (≥ 1.8.10) |
| Published: | 2012-12-11 |
| Author: | Vincent Plagnol |
| Maintainer: | Vincent Plagnol <v.plagnol at ucl.ac.uk> |
| License: | GPL-3 |
| NeedsCompilation: | yes |
| CRAN checks: | ExomeDepth results |
| Package source: | ExomeDepth_0.9.7.tar.gz |
| MacOS X binary: | ExomeDepth_0.9.7.tgz |
| Windows binary: | ExomeDepth_0.9.7.zip |
| Reference manual: | ExomeDepth.pdf |
| Vignettes: |
Using ExomeDepth |
| Old sources: | ExomeDepth archive |