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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
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Document Date: 2014-10-16 09:00:59

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File Size: 673,52 KB

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City

Baltimore / /

Company

Agilent / /

Facility

pipeline etc / Johns Hopkins University / Institute of Genetic Medicine / /

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data processing / /

Organization

Johns Hopkins University / Institute of Genetic Medicine / Kim Doheny Center for Inherited Disease Research / /

Person

Kurt Hetrick / Nara Sobreira / Figure / Hua Ling / Elizabeth Pugh / Dane Witmer / /

ProvinceOrState

Maryland / /

Technology

Genomics / Bioinformatics / /

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http /

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