ExomeCNV is a statistical method to detect CNV and LOH using depth-of-coverage and B-allele frequencies from mapped short sequence reads in exome sequencing data.
| Version: | 1.2 |
| Depends: | DNAcopy |
| Published: | 2011-10-28 |
| Author: | J. Fah Sathirapongsasuti, Hane Lee, and Stanley F. Nelson |
| Maintainer: | J. Fah Sathirapongsasuti <fsathira at fas.harvard.edu> |
| License: | LGPL-2.1 |
| CRAN checks: | ExomeCNV results |
| Package source: | ExomeCNV_1.2.tar.gz |
| MacOS X binary: | ExomeCNV_1.2.tgz |
| Windows binary: | ExomeCNV_1.2.zip |
| Reference manual: | ExomeCNV.pdf |
| Old sources: | ExomeCNV archive |