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2 Article(s) on File
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SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data
Wei Z,
Wang W,
Hu P,
Lyon GJ,
Hakonarson H

Nucleic Acids Res
  39 (19): e132; Oct 2011  
[DOI] [Full Text]

Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications
Lyon GJ,
Jiang T,
Van Wijk R,
Wang W,
Bodily PM,
Xing J,
Tian L,
Robison RJ,
Clement M,
Lin Y,
Zhang P,
Liu Y,
Moore B,
Glessner JT,
Elia J,
Reimherr F,
van Solinge WW,
Yandell M,
Hakonarson H,
Wang J,
Johnson WE,
Wei Z,
Wang K

Discov Med
  12 (62): 41-55; Jul 2011  

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