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Identification of genetic variants using bar-coded multiplexed sequencing

✍ Scribed by Craig, David W; Pearson, John V; Szelinger, Szabolcs; Sekar, Aswin; Redman, Margot; Corneveaux, Jason J; Pawlowski, Traci L; Laub, Trisha; Nunn, Gary; Stephan, Dietrich A

Book ID: 109935334
Publisher: Nature Publishing Group
Year: 2008
Tongue: English
Weight: 687 KB
Volume: 5
Category: Article
ISSN: 1552-4450
DOI: 10.1038/nmeth.1251

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## Abstract Next‐generation sequencing technology allows investigation of both common and rare variants in humans. Exomes are sequenced on the population level or in families to further study the genetics of human diseases. Genetic Analysis Workshop 17 (GAW17) provided exomic data from the 1000 Gen