Center-Authored Papers

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Zheng X, Levine D, Shen J, Gogarten SM, Laurie C, Weir BS.  2012.  A High-performance Computing Toolset for Relatedness and Principal Component Analysis of SNP Data.. Bioinformatics (Oxford, England). 28(24):3326-3328. Abstract
Zheng X, Gogarten SM, Lawrence M, Stilp A, Conomos MP, Weir BS, Laurie C, Levine D.  2017.  SeqArray - A storage-efficient high-performance data format for WGS variant calls.. Bioinformatics (Oxford, England). Abstract
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Teerlink CC, Leongamornlert D, Dadaev T, Thomas A, Farnham J, Stephenson RA, Riska S, McDonnell SK, Schaid DJ, Catalona WJ et al..  2016.  Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.. Human genetics. Abstract
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Landi MT, Chatterjee N, Yu K, Goldin LR, Goldstein AM, Rotunno M, Mirabello L, Jacobs K, Wheeler W, Yeager M et al..  2009.  A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.. American journal of human genetics. 85(5):679-91. Abstract
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Bookman EB, Din-Lovinescu C, Worrall BB, Manolio TA, Bennett SN, Laurie C, Mirel DB, Doheny KF, Anderson GL, Wehr K et al..  2013.  Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).. Genome medicine. 5(1):7. Abstract