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BMC Proceedings|December 19, 2014
Integrated statistical and pathway approach to next-generation sequencing analysis: a family-based study of hypertensionJeremy S Edwards, Susan R Atlas, Susan M Wilson, et al.BMC Proceedings|December 19, 2014
Application of family-based tests of association for rare variants to pathwaysBrian Greco, Alexander Luedtke, Allison Hainline, et al.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.Pageof 102