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3 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  
[Abstract]
[DOI] [Full Text]

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency
Rope AF,
Wang K,
Evjenth R,
Xing J,
Johnston JJ,
Swensen JJ,
Johnson WE,
Moore B,
Huff CD,
Bird LM,
Carey JC,
Opitz JM,
Stevens CA,
Jiang T,
Schank C,
Fain HD,
Robison R,
Dalley B,
Chin S,
South ST,
Pysher TJ,
Jorde LB,
Hakonarson H,
Lillehaug JR,
Biesecker LG,
Yandell M,
Arnesen T,
Lyon GJ

Am J Hum Genet
  89 (1): 28-43; Jul 15 2011  
[Abstract]
[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  
[Abstract]



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