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BMC Proceedings|December 19, 2014
Collapsing singletons may boost signal for associating rare variants in sequencing studyWei Wang, Zhi WeiBMC Proceedings|December 19, 2014
Does the inclusion of rare variants improve risk prediction?Erin Austin, Wei Pan, Xiaotong ShenBMC Proceedings|December 19, 2014
Testing for associations between systolic blood pressure and single-nucleotide polymorphism profiles obtained from sparse principal component analysisAshley Bonner, Binod Neupane, Joseph BeyeneBMC Proceedings|December 19, 2014
Comparing logistic regression, support vector machines, and permanental classification methods in predicting hypertensionHsin-Hsiung Huang, Tu Xu, Jie YangBMC Proceedings|December 19, 2014
Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association testCates Mallaney, Yun Ju SungBMC Proceedings|December 19, 2014
Pedigree-based random effect tests to screen gene pathwaysMarcio Almeida, Juan M Peralta, Vidya Farook, et al.BMC Proceedings|December 19, 2014
Whole genome sequence analysis of the simulated systolic blood pressure in Genetic Analysis Workshop 18 family data: long-term average and collapsing methodsYun Ju Sung, Jacob Basson, Dabeeru C RaoBMC Proceedings|December 19, 2014
Identity-by-descent graphs offer a flexible framework for imputation and both linkage and association analysesElizabeth Marchani Blue, Charles Yk Cheung, Christopher G Glazner, et al.BMC Proceedings|December 19, 2014
Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data setValentina V Pilipenko, Hua He, Brad G Kurowski, et al.BMC Proceedings|December 19, 2014
On family-based genome-wide association studies with large pedigrees: observations and recommendationsDavid W Fardo, Xue Zhang, Lili Ding, et al.Pageof 101