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BMC Proceedings|December 19, 2014
Small sample properties of rare variant analysis methodsMichael D Swartz, Taebeom Kim, Jiangong Niu, et al.BMC Proceedings|December 19, 2014
Higher criticism approach to detect rare variants using whole genome sequencing dataJing Xuan, Li Yang, Zheyang WuBMC Proceedings|December 19, 2014
Imputation in families using a heuristic phasing approachAugust N Blackburn, Angela K Dean, Donna M LehmanBMC Proceedings|December 19, 2014
Joint analysis of sequence data and single-nucleotide polymorphism data using pedigree information for imputation and recombination inferenceSunah Song, Robert Shields, Xin Li, et al.BMC Proceedings|December 19, 2014
PREST-plus identifies pedigree errors and cryptic relatedness in the GAW18 sample using genome-wide SNP dataLei Sun, Apostolos DimitromanolakisBMC Proceedings|December 19, 2014
A generalized least-squares framework for rare-variant analysis in family dataDalin Li, Jerome I Rotter, Xiuqing GuoBMC Proceedings|December 19, 2014
Gene-based analysis of rare and common variants to determine association with blood pressureXiaofeng Liu, Joseph BeyeneBMC Proceedings|December 19, 2014
A penalized linear mixed model for genomic prediction using pedigree structuresCan Yang, Cong Li, Mengjie Chen, et al.BMC Proceedings|December 19, 2014
Considering interactive effects in the identification of influential regions with extremely rare variants via fixed bin approachMichael Agne, Chien-Hsun Huang, Inchi Hu, et al.BMC Proceedings|December 19, 2014
Genetic association analysis for common variants in the Genetic Analysis Workshop 18 data: a Dirichlet regression approachOsvaldo Espin-Garcia, Xiaowei Shen, Xin Qiu, et al.Pageof 102