CNVrd2 - CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.
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.
Last updated 4 months ago
copynumbervariationsnpsequencingsoftwarecoveragelinkagedisequilibriumclustering.
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