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Whole exome capture in solution with 3 Gbp of data
Authors:Matthew N Bainbridge  Min Wang  Daniel L Burgess  Christie Kovar  Matthew J Rodesch  Mark D'Ascenzo  Jacob Kitzman  Yuan-Qing Wu  Irene Newsham  Todd A Richmond  Jeffrey A Jeddeloh  Donna Muzny  Thomas J Albert  Richard A Gibbs
Institution:1. Human Genome Sequencing Center, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, 77030, USA
2. Department of Structural and Computational Biology and Molecular Biophysics, Baylor College of Medicine, One Baylor Plaza, Houston, Texas, 77030, USA
3. Roche NimbleGen, Inc, 504 S. Rosa Road, Madison, WI, 53719, USA
Abstract:We have developed a solution-based method for targeted DNA capture-sequencing that is directed to the complete human exome. Using this approach allows the discovery of greater than 95% of all expected heterozygous singe base variants, requires as little as 3 Gbp of raw sequence data and constitutes an effective tool for identifying rare coding alleles in large scale genomic studies.
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