bioconductor-cnvrd2
CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
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Description
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.
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Summary
CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
Last Updated
Dec 31, 2024 at 14:33
License
GPL-2
Total Downloads
21.6K
Supported Platforms
noarch