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BMC Proceedings|March 1, 2012
Exploration and comparison of methods for combining population- and family-based genetic association using the Genetic Analysis Workshop 17 mini-exomeDavid W Fardo, Anthony R Druen, Jinze Liu, et al.BMC Proceedings|March 1, 2012
Evaluating methods for the analysis of rare variants in sequence dataAlexander Luedtke, Scott Powers, Ashley Petersen, et al.BMC Proceedings|March 1, 2012
Case-control association testing by graphical modeling for the Genetic Analysis Workshop 17 mini-exome sequence dataHaley J Abel, Alun ThomasBMC Proceedings|March 1, 2012
A LASSO-based approach to analyzing rare variants in genetic association studiesJennifer S Brennan, Yunxiao He, Rose Calixte, et al.BMC Proceedings|March 1, 2012
A method to detect single-nucleotide polymorphisms accounting for a linkage signal using covariate-based affected relative pair linkage analysisYeunjoo E Song, Junghyun Namkung, Robert W Shields, et al.BMC Proceedings|March 1, 2012
Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimatesLaura L Faye, Shelley B BullBMC Proceedings|March 1, 2012
Gene-based Higher Criticism methods for large-scale exonic single-nucleotide polymorphism dataShiquan He, Zheyang WuBMC Proceedings|March 1, 2012
Principal components ancestry adjustment for Genetic Analysis Workshop 17 dataJing Jin, Jane E Cerise, Sun Jung Kang, et al.BMC Proceedings|March 1, 2012
Performance of random forests and logic regression methods using mini-exome sequence dataYoonhee Kim, Qing Li, Cheryl D Cropp, et al.BMC Proceedings|March 1, 2012
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regressionHeejong Sung, Yoonhee Kim, Juanliang Cai, et al.Pageof 101