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BMC Proceedings|December 19, 2014
Dynamic pathway analysis of genes associated with blood pressure using whole genome sequence dataPingzhao Hu, Andrew D PatersonBMC Proceedings|December 19, 2014
False-positive rates in two-point parametric linkage analysisSilke Szymczak, Claire L Simpson, Cheryl D Cropp, et al.BMC Proceedings|December 19, 2014
Analysis of homozygosity disequilibrium using whole-genome sequencing dataHsin-Chou Yang, Han-Wei LiBMC Proceedings|December 19, 2014
Evaluating the concordance between sequencing, imputation and microarray genotype calls in the GAW18 dataAlly Rogers, Andrew Beck, Nathan L TintleBMC Proceedings|December 19, 2014
De novo mutations discovered in 8 Mexican American families through whole genome sequencingHeming Wang, Xiaofeng ZhuBMC Proceedings|December 19, 2014
Extended T(2) tests for longitudinal family data in whole genome sequencing studiesYiwei Liu, Jing Xuan, Zheyang WuBMC Proceedings|December 19, 2014
Adjusting for population stratification and relatedness with sequencing dataYiwei Zhang, Wei PanBMC Proceedings|December 19, 2014
Testing optimally weighted combination of variants for hypertensionXingwang Zhao, Qiuying Sha, Shuanglin Zhang, et al.BMC Proceedings|December 19, 2014
Discovering pure gene-environment interactions in blood pressure genome-wide association studies data: a two-step approach incorporating new statisticsMaggie Haitian Wang, Chien-Hsun Huang, Tian Zheng, et al.BMC Proceedings|December 19, 2014
A comparison of two collapsing methods in different approachesCarmen Dering, Arne Schillert, Inke R König, et al.Pageof 101