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BMC Proceedings|December 19, 2014
Evaluation of gene-based association tests for analyzing rare variants using Genetic Analysis Workshop 18 dataAndriy Derkach, Jerry F Lawless, Daniele Merico, 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.Genetic Epidemiology|October 4, 2012
Robust and powerful tests for rare variants using Fisher's method to combine evidence of association from two or more complementary testsAndriy Derkach, Jerry F Lawless, Lei SunBMC Proceedings|December 19, 2014
Using a Bayesian latent variable approach to detect pleiotropy in the Genetic Analysis Workshop 18 dataLizhen Xu, Radu V Craiu, Andriy Derkach, et al.Plos Genetics|May 31, 2022
Major sex differences in allele frequencies for X chromosomal variants in both the 1000 Genomes Project and gnomADZhong Wang, Lei Sun, Andrew D PatersonAmerican Journal of Human Genetics|June 11, 2019
Fast and Accurate Shared Segment Detection and Relatedness Estimation in Un-phased Genetic Data via TRUFFLEApostolos Dimitromanolakis, Andrew D Paterson, Lei SunPlos Genetics|April 24, 2024
Better together against genetic heterogeneity: A sex-combined joint main and interaction analysis of 290 quantitative traits in the UK BiobankBoxi Lin, Andrew D Paterson, Lei SunBMC Genetics|February 21, 2004
Transmission ratio distortion in families from the Framingham Heart StudyAndrew D Paterson, Lei Sun, Xiao-Qing Liu, et al.BMC Proceedings|May 10, 2008
The multiplicity problem in linkage analysis of gene expression data - the power of differentiating cis- and trans-acting regulatorsBaisong Huang, Jagadish Rangrej, Andrew D Paterson, et al.Diabetes|January 6, 2025
Integrative Proteogenomic Analyses Provide Novel Interpretations of Type 1 Diabetes Risk Loci Through Circulating ProteinsTianyuan Lu, Despoina Manousaki, Lei Sun, et al.Pageof 338