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BMC Proceedings|December 17, 2016
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19John Blangero, Tanya M Teslovich, Xueling Sim, et al.BMC Proceedings|December 17, 2016
Genetic complexity at expression quantitative trait lociRita M Cantor, Calvin Pan, Kimberly SiegmundBMC Proceedings|December 17, 2016
Association of genetic variations and gene expression in a family-based studyAchilleas N Pitsillides, Seung-Hoan Choi, John D Hogan, et al.BMC Proceedings|December 17, 2016
Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 dataEmily R Holzinger, Silke Szymczak, James Malley, et al.BMC Proceedings|December 17, 2016
A general method for combining different family-based rare-variant tests of association to improve power and robustness of a wide range of genetic architecturesAlden Green, Kaitlyn Cook, Kelsey Grinde, et al.BMC Proceedings|December 17, 2016
Comparison of multiple single-nucleotide variant association tests in a meta-analysis of Genetic Analysis Workshop 19 family and unrelated dataShuai Wang, Virginia A Fisher, Yuning Chen, et al.BMC Proceedings|December 17, 2016
A novel statistical method for rare-variant association studies in general pedigreesHuanhuan Zhu, Zhenchuan Wang, Xuexia Wang, et al.BMC Proceedings|December 17, 2016
Imputing rare variants in families using a two-stage approachSamantha Lent, Xuan Deng, L Adrienne Cupples, et al.BMC Proceedings|December 17, 2016
Prioritization of family member sequencing for the detection of rare variantsRachel Sippy, Jill M Kolesar, Burcu F Darst, et al.BMC Proceedings|December 17, 2016
Testing rare variants for hypertension using family-based tests with different weighting schemesXuexia Wang, Xingwang Zhao, Jin ZhouPageof 101