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BMC Proceedings|March 1, 2012
Identification of genes and variants associated with quantitative traits using Bayesian factor screeningKith Pradhan, Seungtai Chris Yoon, Tao Wang, et al.BMC Proceedings|March 1, 2012
Detection of rare variant effects in association studies: extreme values, iterative regression, and a hybrid approachZhaogong Zhang, Qiuying Sha, Xinli Wang, et al.BMC Proceedings|March 1, 2012
Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 dataYauheniya Cherkas, Nandini Raghavan, Stephan Francke, et al.BMC Proceedings|March 1, 2012
Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 dataAldi T Kraja, Jacek Czajkowski, Mary F Feitosa, et al.BMC Proceedings|March 1, 2012
LASSO model selection with post-processing for a genome-wide association study data setAllan J Motyer, Chris McKendry, Sally Galbraith, et al.BMC Proceedings|March 1, 2012
Stratify or adjust? Dealing with multiple populations when evaluating rare variantsRobert C Culverhouse, Anthony L Hinrichs, Brian K SuarezBMC Proceedings|March 1, 2012
Identifying influential regions in extremely rare variants using a fixed-bin approachMichael Agne, Chien-Hsun Huang, Inchi Hu, et al.BMC Proceedings|March 1, 2012
Application of collapsing methods for continuous traits to the Genetic Analysis Workshop 17 exome sequence dataYun Ju Sung, Treva K Rice, Dabeeru C RaoBMC Proceedings|March 1, 2012
Do rare variant genotypes predict common variant genotypes?Jack W Kent, Vidya Farook, Harald Hh Göring, et al.BMC Proceedings|March 1, 2012
Comparative study of statistical methods for detecting association with rare variants in exome-resequencing dataMohamad Saad, Aude Saint Pierre, Nora Bohossian, et al.Pageof 102