ParseCNV is a tool to associate copy number variation (CNV) in case-control design and family-based studies. The ParseCNV algorithm also implements quality control.
Genetics; population genetics; genetic variation
Chih-Hao Chen, Hsing-Chung Lee, Qingdong Ling, Hsiao-Rong Chen, Yi-An Ko, Tsong-Shan Tsou, Sun-Chong Wang, Li-Ching Wu, H. C. Lee "ParseCNV integrative copy number variation association software with quality tracking" Nucleic Acids Research, Volume 39, Issue 13, 1 July 2011, Page e89 https://doi.org/10.1093/nar/gks1346
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