A Matlab tool for detection and localization of copy number variation (CNV).
Oncology; Genetic variation; Sequencing
Chiang DY, Getz G, Jaffe DB, O'Kelly MJ, Zhao X, Carter SL, Russ C, Nusbaum C, Meyerson M, Lander ES "High-resolution mapping of copy-number alterations with massively parallel sequencing." Nat Methods. 2009 Jan;6(1):99-103. https://doi.org/10.1038/nmeth.1276
PMID: 19043412
PMCID: PMC2630795
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