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Genetic Epidemiology|June 19, 2003
Finding starting points for Markov chain Monte Carlo analysis of genetic data from large and complex pedigreesYuqun Luo, Shili LinGenetic Epidemiology|August 19, 2006
A comparison of methods for intermediate fine mappingCharalampos Papachristou, Shili LinGenetic Epidemiology|November 26, 2008
Generalized linear modeling with regularization for detecting common disease rare haplotype associationWei Guo, Shili LinBiorxiv : the Preprint Server for Biology|July 16, 2025
Can Random Walking on a Hi-C Contact Matrix Lead to Data Quality Improvement? An AssessmentYongqi Liu, Shili LinPlos One|January 17, 2024
An in silico procedure for generating protein-mediated chromatin interaction data and comparison of significant interaction calling methodsShuyuan Lou, Shili LinBiometrics|October 20, 2011
Likelihood approach for detecting imprinting and in utero maternal effects using general pedigrees from prospective family-based association studiesJingyuan Yang, Shili LinHuman Heredity|April 2, 2005
A confidence set inference procedure for gene mapping using markers with incomplete polymorphismCharalampos Papachristou, Shili LinBiometrics|April 6, 2013
Regularization in finite mixture of regression models with diverging number of parametersAbbas Khalili, Shili LinBiometrics|May 24, 2016
A random effect model for reconstruction of spatial chromatin structureJincheol Park, Shili LinBMC Proceedings|December 19, 2014
Detecting longitudinal effects of haplotypes and smoking on hypertension using B-splines and Bayesian LASSOShuang Xia, Shili LinPageof 111