A tool to detect copy number variation (CNV). CNVer algorithm uses paired-end, matepair, information together with the donor graph framework to adjust coverage for localized sequencing biases.
Mapping; Sequencing; Genetic variation; Software engineering
Medvedev P, Fiume M, Dzamba M, Smith T, Brudno M "Detecting copy number variation with mated short reads." Genome Res. 2010 Nov;20(11):1613-22. https://doi.org/10.1101/gr.106344.110
PMID: 20805290
PMCID: PMC2963824
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