Rare variant association test in family-based sequencing studies. - Xuefeng Wang; Zhenyu Zhang; Nathan Morris; Tianxi Cai; Seunggeun Lee; Chaolong Wang; Timothy W. Yu; Christopher A. Walsh; Xihong Lin (Briefings Bioinform., 2017)

LLR: a latent low-rank approach to colocalizing genetic risk variants in multiple GWAS. - Jin Liu 011; Xiang Wan; Chaolong Wang; Chao Yang; Xiaowei Zhou 001; Can Yang 002 (Bioinform., 2017)

LASER server: ancestry tracing with genotypes or sequence reads. - Daniel Taliun; Sonia P. Chothani; Sebastian Schönherr; Lukas Forer; Michael Boehnke; Gonçalo R. Abecasis; Chaolong Wang (Bioinform., 2017)

Using off-target data from whole-exome sequencing to improve genotyping accuracy, association analysis and polygenic risk prediction. - Jinzhuang Dou; Degang Wu; Lin Ding; Kai Wang; Minghui Jiang 005; Xiaoran Chai; Dermot F. Reilly; E. Shyong Tai; Jianjun Liu; Xueling Sim; Shanshan Cheng; Chaolong Wang (Briefings Bioinform., 2021)

Rare variant association tests for ancestry-matched case-control data based on conditional logistic regression. - Shanshan Cheng; Jingjing Lyu; Xian Shi; Kai Wang; Zengmiao Wang; Minghua Deng; Baoluo Sun; Chaolong Wang (Briefings Bioinform., 2022)

Identification of genomic regions distorting population structure inference in diverse continental groups. - Qiuxuan Liu; Degang Wu; Chaolong Wang (Quant. Biol., 2022)

MethylGenotyper: Accurate Estimation of SNP Genotypes and Genetic Relatedness from DNA Methylation Data. - Yi Jiang; Minghan Qu; Minghui Jiang; Xuan Jiang; Shane Fernandez; Tenielle Porter; Simon M. Laws; Colin L. Masters; Huan Guo; Shanshan Cheng; Chaolong Wang (Genom. Proteom. Bioinform., 2024)