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BMC Proceedings|March 1, 2012
Enhancing the discovery of rare disease variants through hierarchical modelingGary K ChenBMC Proceedings|March 1, 2012
Rare variant density across the genome and across populationsPaola Raska, Xiaofeng ZhuBMC Proceedings|March 1, 2012
Search for compound heterozygous effects in exome sequence of unrelated subjectsG Bryce Christensen, Christophe G LambertBMC Proceedings|March 1, 2012
Pathway analysis for family data using nested random-effects modelsJeanine J Houwing-Duistermaat, Hae-Won Uh, Roula TsonakaBMC Proceedings|March 1, 2012
A weighted accumulation test for associating rare genetic variation with quantitative phenotypesChuanhua Xing, Glen A Satten, Andrew S AllenBMC Proceedings|March 1, 2012
Region-based and pathway-based QTL mapping using a p-value combination methodHsin-Chou Yang, Chia-Wei ChenBMC Proceedings|March 1, 2012
Enriching rare variants using family-specific linkage informationGang Shi, Jeannette Simino, Dabeeru C RaoBMC Proceedings|March 1, 2012
Identification of genes associated with complex traits by testing the genetic dissimilarity between individualsYan V Sun, Wei Zhao, Kerby A Shedden, et al.BMC Proceedings|March 1, 2012
Novel tree-based method to generate markers from rare variant dataYuan Jiang, Jennifer S Brennan, Rose Calixte, et al.BMC Proceedings|March 1, 2012
Challenges and directions: an analysis of Genetic Analysis Workshop 17 data by collapsing rare variants within family dataPeng Lin, Michael Hamm, Sarah Hartz, et al.Pageof 102