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BMC Genetics|January 8, 2011
A powerful hybrid approach to select top single-nucleotide polymorphisms for genome-wide association studyJian Wang, Sanjay SheteStatistical Methods in Medical Research|January 31, 2017
Estimation of indirect effect when the mediator is a censored variableJian Wang, Sanjay SheteBMC Medical Informatics and Decision Making|July 20, 2016
Using the weighted area under the net benefit curve for decision curve analysisRajesh Talluri, Sanjay SheteBMC Medical Research Methodology|September 1, 2016
Time-varying SMART design and data analysis methods for evaluating adaptive intervention effectsTianjiao Dai, Sanjay SheteHuman Heredity|October 24, 2006
TLINKAGE-IMPRINT: a model-based approach to performing two-locus genetic imprinting analysisSanjay Shete, Xiaojun ZhouPlos One|November 24, 2011
Testing Hardy-Weinberg proportions in a frequency-matched case-control genetic association studyJian Wang, Sanjay SheteBMC Proceedings|December 19, 2014
Gaussian graphical models for phenotypes using pedigree data and exploratory analysis using networks with genetic and nongenetic factors based on Genetic Analysis Workshop 18 dataRajesh Talluri, Sanjay SheteCancer Informatics|March 4, 2015
Evaluating methods for modeling epistasis networks with application to head and neck cancerRajesh Talluri, Sanjay SheteMethods in Molecular Biology (Clifton, N.J.)|February 7, 2012
Testing departure from Hardy-Weinberg proportionsJian Wang, Sanjay SheteGenetic Epidemiology|July 20, 2011
Power and type I error results for a bias-correction approach recently shown to provide accurate odds ratios of genetic variants for the secondary phenotypes associated with primary diseasesJian Wang, Sanjay ShetePageof 32