CNVrd2-package


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.<p></p><p></p>

 package

CNVrd2 uses next-generation sequencing data to measure human gene copy number for multiple samples,
indentify SNPs tagging copy number variants and detect copy
number polymorphic genomic regions.

Hoang Tan Nguyen

CNVrd2

CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.

CNVrd2-package function

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.

CNVrd2-package: CNVrd2

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