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BMC Proceedings|March 1, 2012
Application of collapsing methods for continuous traits to the Genetic Analysis Workshop 17 exome sequence dataYun Ju Sung, Treva K Rice, Dabeeru C RaoBMC Proceedings|March 1, 2012
Do rare variant genotypes predict common variant genotypes?Jack W Kent, Vidya Farook, Harald Hh Göring, et al.BMC Proceedings|March 1, 2012
Comparative study of statistical methods for detecting association with rare variants in exome-resequencing dataMohamad Saad, Aude Saint Pierre, Nora Bohossian, et al.BMC Proceedings|March 1, 2012
Enhancing the discovery of rare disease variants through hierarchical modelingGary K ChenBMC Proceedings|March 1, 2012
Rare variant density across the genome and across populationsPaola Raska, Xiaofeng ZhuBMC Proceedings|March 1, 2012
Search for compound heterozygous effects in exome sequence of unrelated subjectsG Bryce Christensen, Christophe G LambertBMC Proceedings|March 1, 2012
Pathway analysis for family data using nested random-effects modelsJeanine J Houwing-Duistermaat, Hae-Won Uh, Roula TsonakaBMC Proceedings|March 1, 2012
A weighted accumulation test for associating rare genetic variation with quantitative phenotypesChuanhua Xing, Glen A Satten, Andrew S AllenBMC Proceedings|March 1, 2012
Region-based and pathway-based QTL mapping using a p-value combination methodHsin-Chou Yang, Chia-Wei ChenBMC Proceedings|March 1, 2012
Enriching rare variants using family-specific linkage informationGang Shi, Jeannette Simino, Dabeeru C RaoPageof 101