CNVrd2-package {CNVrd2} | R Documentation |
CNVrd2 uses next-generation sequencing data to measure human gene copy number for multiple samples and indentify SNPs/INDELs which are in linkage disequilibrium with the gene copy number variation.
Package: | CNVrd2 |
Type: | Package |
Version: | 1.0 |
Date: | 2013-03-26 |
License: | GPL-2 |
Depends: | methods |
Maintainer: Hoang Tan Nguyen <hoangtannguyenvn@gmail.com>