a scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries建设一个可伸缩,完全自动化的过程sequence-ready人类外显子组捕获库目标.pdfVIP
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a scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries建设一个可伸缩,完全自动化的过程sequence-ready人类外显子组捕获库目标
Fisher et al. Genome Biology 2011, 12:R1
/2011/12/1/R1
METHOD Open Access
A scalable, fully automated process for
construction of sequence-ready human exome
targeted capture libraries
1 1 1 1 1 1 1
Sheila Fisher , Andrew Barry , Justin Abreu , Brian Minie , Jillian Nolan , Toni M Delorey , Geneva Young ,
1 1 1 2 3 3
Timothy J Fennell , Alexander Allen , Lauren Ambrogio , Aaron M Berlin , Brendan Blumenstiel , Kristian Cibulskis ,
1 1 4 1 1 1 2
Dennis Friedrich , Ryan Johnson , Frank Juhn , Brian Reilly , Ramy Shammas , John Stalker , Sean M Sykes ,
1 1 1 1,4 2 1 2*
Jon Thompson , John Walsh , Andrew Zimmer , Zac Zwirko , Stacey Gabriel , Robert Nicol , Chad Nusbaum
Abstract
Genome targeting methods enable cost-effective capture of specific subsets of the genome for sequencing. We
present here an automated, highly scalable method for carrying out the Solution Hybrid Selection capture
approach that provides a dramatic increase in scale and throughput of sequence-ready libraries produced.
Significant process improvements and a series of in-process quality control checkpoints are also added. These
process improvements can also be used in a manual version of the protocol.
Background and including the targeted capture step, the all-in cost
The cost of DNA sequencing co
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