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BMC Proceedings|December 17, 2016
A general method for combining different family-based rare-variant tests of association to improve power and robustness of a wide range of genetic architecturesAlden Green, Kaitlyn Cook, Kelsey Grinde, et al.BMC Proceedings|December 17, 2016
Comparison of multiple single-nucleotide variant association tests in a meta-analysis of Genetic Analysis Workshop 19 family and unrelated dataShuai Wang, Virginia A Fisher, Yuning Chen, et al.BMC Proceedings|December 17, 2016
A novel statistical method for rare-variant association studies in general pedigreesHuanhuan Zhu, Zhenchuan Wang, Xuexia Wang, et al.BMC Proceedings|December 17, 2016
Imputing rare variants in families using a two-stage approachSamantha Lent, Xuan Deng, L Adrienne Cupples, et al.BMC Proceedings|December 17, 2016
Prioritization of family member sequencing for the detection of rare variantsRachel Sippy, Jill M Kolesar, Burcu F Darst, et al.BMC Proceedings|December 17, 2016
Testing rare variants for hypertension using family-based tests with different weighting schemesXuexia Wang, Xingwang Zhao, Jin ZhouBMC Proceedings|December 17, 2016
Powerful association test combining rare variant and gene expression using family data from Genetic Analysis Workshop 19Yen-Yi Ho, Weihua Guan, Michael O'Connell, et al.BMC Proceedings|December 17, 2016
Identity-by-descent mapping for diastolic blood pressure in unrelated Mexican AmericansXiao-Qing Liu, Jillian Fazio, Pingzhao Hu, et al.BMC Proceedings|December 17, 2016
Comparing strategies for combined testing of rare and common variants in whole sequence and genome-wide genotype dataDörthe Malzahn, Stefanie Friedrichs, Heike BickeböllerBMC Proceedings|December 17, 2016
Identity-by-descent estimation with population- and pedigree-based imputation in admixed family dataMohamad Saad, Alejandro Q Nato, Fiona L Grimson, et al.Pageof 102