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Genetic Epidemiology|December 1, 2011
Association of direct-to-consumer genome-wide disease risk estimates and self-reported diseaseCinnamon S Bloss, Eric J Topol, Nicholas J SchorkGenetic Epidemiology|December 1, 2011
Detecting multiple causal rare variants in exome sequence dataKenny Q Ye, Corinne D EngelmanGenetic Epidemiology|December 1, 2011
Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17Nathan Tintle, Hugues Aschard, Inchi Hu, et al.Genetic Epidemiology|December 1, 2011
Rare variants, common markers: synthetic association and beyondJack W KentGenetic Epidemiology|November 30, 2011
PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity dataNatsuhiko Kumasaka, Hironori Fujisawa, Naoya Hosono, et al.Genetic Epidemiology|October 20, 2011
Incorporating model uncertainty in detecting rare variants: the Bayesian risk indexMelanie A Quintana, Jonine L Berstein, Duncan C Thomas, et al.Genetic Epidemiology|February 8, 2012
Gene-environment interactions on growth trajectoriesShuang Wang, Wei Xiong, Weiping Ma, et al.Genetic Epidemiology|February 8, 2012
Genetic epidemiology with a capital E: where will we be in another 10 years?Duncan C ThomasGenetic Epidemiology|July 20, 2011
Detection of cis-acting regulatory SNPs using allelic expression dataRui Xiao, Laura J ScottGenetic Epidemiology|July 20, 2011
Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV arrayNiall Cardin, Chris Holmes, , et al.Pageof 285