CNVrd2-package: CNVrd2
In CNVrd2: CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
Description
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.
Details
Package: CNVrd2
Type: Package
Version: 1.0
Date: 2013-03-26
License: GPL-2
Depends: methods
Author(s)
Maintainer: Hoang Tan Nguyen <hoangtannguyenvn@gmail.com>
CNVrd2 documentation built on Nov. 8, 2020, 5:30 p.m.
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Description
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.
Details
| Package: | CNVrd2 |
| Type: | Package |
| Version: | 1.0 |
| Date: | 2013-03-26 |
| License: | GPL-2 |
| Depends: | methods |
Author(s)
Maintainer: Hoang Tan Nguyen <hoangtannguyenvn@gmail.com>
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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