Copy Number Variation (CNV) detection in whole exome sequencing data for Mendelian disorders Peng Zhang, Hua Ling, Elizabeth Pugh, Kurt Hetrick, Dane Witmer, Nara Sobreira, David Valle, Kim Doheny Center for Inherited Di

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Date: 2014-10-16 09:00:59 Copy-number variation DNA sequencing Exome sequencing Full genome sequencing Excavator Medical genetics Center for Applied Genomics Biology Molecular biology Genetics		Copy Number Variation (CNV) detection in whole exome sequencing data for Mendelian disorders Peng Zhang, Hua Ling, Elizabeth Pugh, Kurt Hetrick, Dane Witmer, Nara Sobreira, David Valle, Kim Doheny Center for Inherited Di Add to Reading List Source URL: www.cidr.jhmi.edu Download Document from Source Website File Size: 673,52 KB Share Document on Facebook

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