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BMC Proceedings|March 1, 2012
Family- and population-based designs identify different rare causal variantsXue Zhang, Hua He, Lili Ding, et al.BMC Proceedings|March 1, 2012
Application of Bayesian network structure learning to identify causal variant SNPs from resequencing dataChristopher E Schlosberg, Tae-Hwi Schwantes-An, Weimin Duan, et al.BMC Proceedings|March 1, 2012
Use of Bayesian networks to dissect the complexity of genetic disease: application to the Genetic Analysis Workshop 17 simulated dataJia Kang, Wei Zheng, Lun Li, et al.BMC Proceedings|March 1, 2012
Does pathway analysis make it easier for common variants to tag rare ones?Hae-Won Uh, Roula Tsonaka, Jeanine J Houwing-DuistermaatBMC Proceedings|March 1, 2012
Gene-based multiple trait analysis for exome sequencing dataJingyuan Zhao, Anbupalam ThalamuthuBMC Proceedings|March 1, 2012
Improved power by collapsing rare and common variants based on a data-adaptive forward selection strategyYilin Dai, Ling Guo, Jianping Dong, et al.BMC Proceedings|March 1, 2012
Comparison of SNP-based and gene-based association studies in detecting rare variants using unrelated individualsLiping Tong, Bamidele Tayo, Jie Yang, et al.BMC Proceedings|March 1, 2012
Resampling procedures to identify important SNPs using a consensus approachChristopher Pardy, Allan Motyer, Susan WilsonBMC Proceedings|March 1, 2012
Comparison of collapsing methods for the statistical analysis of rare variantsCarmen Dering, Andreas Ziegler, Inke R König, et al.BMC Proceedings|May 30, 2012
Genomic selection using regularized linear regression models: ridge regression, lasso, elastic net and their extensionsJoseph O Ogutu, Torben Schulz-Streeck, Hans-Peter PiephoPageof 101