Imputation of coding variants in African Americans: better performance using data from the exome sequencing project. - Qing Duan; Eric Yi Liu; Paul L. Auer; Guosheng Zhang; Ethan M. Lange; Goo Jun; Chris Bizon; Shuo Jiao; Steven Buyske; Nora Franceschini; Chris S. Carlson; Li Hsu; et al. (Bioinform., 2013)

Evaluation of microarray-based DNA methylation measurement using technical replicates: the Atherosclerosis Risk In Communities (ARIC) Study. - Maitreyee Bose; Chong Wu; James S. Pankow; Ellen W. Demerath; Jan Bressler; Myriam Fornage; Megan L. Grove; Thomas H. Mosley Jr.; Chindo Hicks; Kari E. North; Wen Kao; Yu Zhang; et al. (BMC Bioinform., 2014)

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals. - Emily Rose Holzinger; Shefali S. Verma; Carrie Colleen Buchanan Moore; Molly A. Hall; Rishika De; Diane Gilbert-Diamond; Matthew B. Lanktree; Nathan Pankratz; Antoinette Amuzu; Amber Burt; Caroline Dale; Scott M. Dudek; et al. (BioData Min., 2017)

A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. - Xihao Li; Han Chen; Margaret Sunitha Selvaraj; Eric Van Buren; Hufeng Zhou; Yuxuan Wang 008; Ryan Sun; Zachary R. McCaw; Zhi Yu; Min-Zhi Jiang; Daniel DiCorpo; Sheila M. Gaynor; et al. (Nat. Comput. Sci., 2025)