URL: http://www.bioconductor.org/packages/devel/bioc/html/CNVrd2.html
Proper Citation: CNVrd2 (RRID:SCR_001723)
Description: A software package that 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.
Synonyms: CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data
Resource Type: software resource
Defining Citation: PMID:23646200
Keywords: standalone software, illumina, unix/linux, mac os x, windows, r, clustering., copy number variation, coverage, linkage disequilibrium, snp, sequencing
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