A method for identifying haplotypes carrying the causative allele in positive natural selection and genome-wide association studies. - Rick Twee-Hee Ong; Xuanyao Liu; Wan-Ting Poh; Xueling Sim; Kee Seng Chia; Yik-Ying Teo (Bioinform., 2011)

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)

Multidisciplinary Effort to Drive Precision-Medicine for the Future. - Dewei Kong; Haojie Yu; Xueling Sim; Kevin White 008; E. Shyong Tai; Markus Wenk; Adrian Kee Keong Teo (Frontiers Digit. Health, 2022)

Are Traditional Deep Learning Model Approaches as Effective as a Retinal-Specific Foundation Model for Ocular and Systemic Disease Detection? - Samantha Min Er Yew; Xiaofeng Lei; Jocelyn Hui Lin Goh; Yibing Chen; Sahana Srinivasan; Miao-li Chee; Krithi Pushpanathan; Ke Zou; Qingshan Hou; Zhi Da Soh; Cancan Xue; Marco Chak Yan Yu; et al. (CoRR, 2025)