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BMC Proceedings|December 19, 2014
A novel transmission-based test of association for multivariate phenotypes: an application to systolic and diastolic blood pressure levelsTanushree Haldar, Indranil Mukhopadhyay, Saurabh GhoshBMC Proceedings|December 19, 2014
Fast genome-wide pedigree quantitative trait loci analysis using MENDELHua Zhou, Jin Zhou, Eric M Sobel, et al.BMC Proceedings|December 19, 2014
Estimating proportions of explained variance: a comparison of whole genome subsetsStella Aslibekyan, Howard W Wiener, Guodong Wu, et al.BMC Proceedings|December 19, 2014
Genetic Analysis Workshop 18 single-nucleotide variant prioritization based on protein impact, sequence conservation, and gene annotationThomas Nalpathamkalam, Andriy Derkach, Andrew D Paterson, et al.BMC Proceedings|December 19, 2014
Small sample properties of rare variant analysis methodsMichael D Swartz, Taebeom Kim, Jiangong Niu, et al.BMC Proceedings|December 19, 2014
Higher criticism approach to detect rare variants using whole genome sequencing dataJing Xuan, Li Yang, Zheyang WuBMC Proceedings|December 19, 2014
Imputation in families using a heuristic phasing approachAugust N Blackburn, Angela K Dean, Donna M LehmanBMC Proceedings|December 19, 2014
Joint analysis of sequence data and single-nucleotide polymorphism data using pedigree information for imputation and recombination inferenceSunah Song, Robert Shields, Xin Li, et al.BMC Proceedings|December 19, 2014
PREST-plus identifies pedigree errors and cryptic relatedness in the GAW18 sample using genome-wide SNP dataLei Sun, Apostolos DimitromanolakisBMC Proceedings|December 19, 2014
A generalized least-squares framework for rare-variant analysis in family dataDalin Li, Jerome I Rotter, Xiuqing GuoPageof 101