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BMC Proceedings|March 1, 2012
Prioritizing single-nucleotide variations that potentially regulate alternative splicingMingxiang Teng, Yadong Wang, Guohua Wang, et al.BMC Proceedings|March 1, 2012
Strategies for selection of subjects for sequencing after detection of a linkage peakKristina Allen-Brady, James Farnham, Lisa Cannon-AlbrightBMC Proceedings|March 1, 2012
An aggregating U-Test for a genetic association study of quantitative traitsMing Li, Wenjiang Fu, Qing LuBMC Proceedings|December 19, 2014
Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigreesHeike Bickeböller, Julia N Bailey, Joseph Beyene, et al.BMC Proceedings|December 19, 2014
Identification of rare variants for hypertension with incorporation of linkage informationYen-Feng Chiu, Ren-Hua Chung, Chun-Yi Lee, et al.BMC Proceedings|December 19, 2014
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigreesLaura Almasy, Thomas D Dyer, Juan M Peralta, et al.BMC Proceedings|December 19, 2014
A 2-step penalized regression method for family-based next-generation sequencing association studiesXiuhua Ding, Shaoyong Su, Kannabiran Nandakumar, et al.BMC Proceedings|December 19, 2014
Admixture mapping analysis in the context of GWAS with GAW18 dataMengjie Chen, Can Yang, Cong Li, et al.BMC Proceedings|December 19, 2014
Family-based tests applied to extended pedigrees identify rare variants related to hypertensionMengyuan Xu, Harold Z Wang, Wei Guo, et al.BMC Proceedings|December 19, 2014
Identifying cryptic population structure in multigenerational pedigrees in a Mexican American sampleRobert C Culverhouse, Anthony L Hinrichs, Brian K SuarezPageof 101