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Genetic Epidemiology|December 4, 2012
Performance and robustness of penalized and unpenalized methods for genetic prediction of complex human diseaseGad Abraham, Adam Kowalczyk, Justin Zobel, et al.Genetic Epidemiology|January 3, 2013
SNP prioritization using a Bayesian probability of associationJohn R Thompson, Martin Gögele, Christian X Weichenberger, et al.Genetic Epidemiology|January 12, 2013
Importance of different types of prior knowledge in selecting genome-wide findings for follow-upCosetta Minelli, Alessandro De Grandi, Christian X Weichenberger, et al.Genetic Epidemiology|January 16, 2013
Association testing of the mitochondrial genome using pedigree dataChunyu Liu, Josée Dupuis, Martin G Larson, et al.Genetic Epidemiology|September 25, 2014
SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structureRen-Hua Chung, Wei-Yun Tsai, Chang-Hsun Hsieh, et al.Genetic Epidemiology|September 9, 2014
A unified sparse representation for sequence variant identification for complex traitsShaolong Cao, Huaizhen Qin, Hong-Wen Deng, et al.Genetic Epidemiology|January 1, 1990
Familial resemblance of plasma apolipoprotein B: the Nancy studyL Tiret, J Steinmetz, B Herbeth, et al.Genetic Epidemiology|January 1, 1990
Power of the linkage test for a heterogeneous disorder due to two independent inherited causes: a simulation studyM Martinez, L R GoldinGenetic Epidemiology|May 2, 2013
Strategy to control type I error increases power to identify genetic variation using the full biological trajectoryK S Benke, Y Wu, D M Fallin, et al.Genetic Epidemiology|June 7, 2013
Encore: Genetic Association Interaction Network centrality pipeline and application to SLE exome dataNicholas A Davis, Caleb A Lareau, Bill C White, et al.Pageof 285