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BMC Proceedings|March 1, 2012
Disease risk prediction with rare and common variantsChengqing Wu, Kyle M Walsh, Andrew T Dewan, et al.BMC Proceedings|March 1, 2012
Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approachLili Ding, Tesfaye M Baye, Hua He, et al.BMC Proceedings|March 1, 2012
Identifying rare variants using a Bayesian regression approachAimin Yan, Nan M Laird, Cheng LiBMC Proceedings|March 1, 2012
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence dataClaire L Simpson, Cristina M Justice, Mera Krishnan, et al.BMC Proceedings|March 1, 2012
Identification of functional genetic variation in exome sequence analysisAndrew Jaffe, Genevieve Wojcik, Audrey Chu, et al.BMC Proceedings|March 1, 2012
Identification of multiple rare variants associated with a diseaseJeesun Jung, Jessica Dantzer, Yunlong LiuBMC Proceedings|March 1, 2012
Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 dataWenan Chen, Xi Gao, Jiexun Wang, et al.BMC Proceedings|March 1, 2012
Regularized regression method for genome-wide association studiesJin Liu, Kai Wang, Shuangge Ma, et al.BMC Proceedings|March 1, 2012
Genome-wide association analysis of GAW17 data using an empirical Bayes variable selectionVitara Pungpapong, Libo Wang, Yanzhu Lin, et al.BMC Proceedings|March 1, 2012
Identifying variants that contribute to linkage for dichotomous and quantitative traits in extended pedigreesWei-Min Chen, Ani Manichaikul, Stephen S RichPageof 101