ExomeCNV (1.4)
Detect CNV and LOH from Exome Sequencing Data.
http://cran.r-project.org/web/packages/ExomeCNV
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.
Maintainer:
J. Fah Sathirapongsasuti
Author(s): J. Fah Sathirapongsasuti, Hane Lee, and Stanley F. Nelson
License: LGPL-2.1
Uses: Does not use any package
Released 9 months ago.
4 previous versions
- ExomeCNV_1.3. Released 12 months ago.
- ExomeCNV_1.2. Released over 1 year ago.
- ExomeCNV_1.1. Released over 1 year ago.
- ExomeCNV_1.0. Released almost 2 years ago.
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