ExomeDepth uses read count data from exome or targeted sequencing experiments to call copy number variants.
| Package: | ExomeDepth |
| Type: | Package |
| Version: | 0.1 |
| Date: | 2012-02-01 |
| License: | What license is it under? |
| LazyLoad: | yes |
The two key functions are: select.reference.set CallCNVs
A robust model for read count data in exome sequencing experiments and implications for copy number variant calling, Bioinformatics, In Press