Comprehensive variation discovery in single human genomes

Comprehensive variation discovery in single human genomes

Complete knowledge of the genetic variation in individual human genomes is a crucial foundation for understanding the etiology of disease. Genetic variation is typically characterized by sequencing individual genomes and comparing reads to a reference. Existing methods do an excellent job of detecti...

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Bibliographic Details
Main Authors: Weisenfeld, Neil I (Author), Yin, Shuangye (Author), Sharpe, Ted (Author), Lau, Bayo (Author), Hegarty, Ryan (Author), Holmes, Laurie (Author), Sogoloff, Brian (Author), Tabbaa, Diana (Author), Williams, Louise (Author), Russ, Carsten (Author), Nusbaum, Chad (Author), MacCallum, Iain (Author), Jaffe, David B. (Author), Lander, Eric Steven (Author)
Other Authors: Massachusetts Institute of Technology. Department of Biology (Contributor), Lander, Eric S. (Contributor)
Format: Article
Language:English
Published: Nature Publishing Group, 2015-06-05T15:14:06Z.
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