Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth. Fromer, M. , Moran JL , Chambert K. , Banks E. , Bergen SE , Ruderfer DM , Handsaker RE , McCarroll SA , O'Donovan MC , Owen MJ , Kirov G. , Sullivan PF , Hultman CM , Sklar P. , and Purcell SM American journal of human genetics, 2012/10/05, Volume 91, Issue 4, p.597-607, (2012)
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Abstract
zCall: A Rare Variant Caller for Array-based Genotyping. Goldstein, JI , Crenshaw A. , Carey J. , Grant G. , Maguire J. , Fromer M. , O'Dushlaine C. , Moran JL , Chambert K. , Stevens C. , Swedish Schizophrenia Consortium , ARRA Autism Sequencing Consortium , Sklar P. , Hultman CM , Purcell S. , McCarroll S. , Sullivan PF , Daly M. J. , and Neale BM Bioinformatics (Oxford, England), 2012/07/27, (2012)
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Abstract
Patterns and rates of exonic de novo mutations in autism spectrum disorders. Neale, BM , Kou Y. , Liu L. , Ma'ayan A. , Samocha KE , Sabo A. , Lin CF , Stevens C. , Wang LS , Makarov V. , Polak P. , Yoon S. , Maguire J. , Crawford EL , Campbell NG , Geller ET , Valladares O. , Schafer C. , Liu H. , Zhao T. , et al. Nature, 2012/04/04, (2012)
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Abstract
