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Plos Computational Biology|June 14, 2013
Leveraging prior information to detect causal variants via multi-variant regressionNanye Long, Samuel P Dickson, Jessica M Maia, et al.American Journal of Human Genetics|April 5, 2011
A genome-wide comparison of the functional properties of rare and common genetic variants in humansQianqian Zhu, Dongliang Ge, Jessica M Maia, et al.Genomics|August 2, 2011
A whole-genome analysis of premature termination codonsElizabeth T Cirulli, Erin L Heinzen, Fred S Dietrich, et al.Genome Biology|July 6, 2010
Screening the human exome: a comparison of whole genome and whole transcriptome sequencingElizabeth T Cirulli, Abanish Singh, Kevin V Shianna, et al.Plos One|July 15, 2017
Evaluating whole genome sequence data from the Genetic Absence Epilepsy Rat from Strasbourg and its related non-epileptic strainPablo M Casillas-Espinosa, Kim L Powell, Mingfu Zhu, et al.Plos One|April 12, 2022
A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis populationIan R White, Sarah E Kleinstein, Christophe Praet, et al.Proceedings of the National Academy of Sciences of the United States of America|April 21, 2010
Diversification in the genetic architecture of gene expression and transcriptional networks in organ differentiation of PopulusDerek R Drost, Catherine I Benedict, Arthur Berg, et al.American Journal of Human Genetics|September 4, 2012
Prioritizing genetic variants for causality on the basis of preferential linkage disequilibriumQianqian Zhu, Dongliang Ge, Erin L Heinzen, et al.Plos Biology|February 19, 2009
Tissue-specific genetic control of splicing: implications for the study of complex traitsErin L Heinzen, Dongliang Ge, Kenneth D Cronin, et al.The Journal of Infectious Diseases|March 9, 2010
Host determinants of HIV-1 control in African AmericansKimberly Pelak, David B Goldstein, Nicole M Walley, et al.Pageof 2