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2020 – today
- 2024
[j7]Yi Jiang, Minghan Qu, Minghui Jiang, Xuan Jiang, Shane Fernandez, Tenielle Porter, Simon M. Laws, Colin L. Masters, Huan Guo, Shanshan Cheng, Chaolong Wang:
MethylGenotyper: Accurate Estimation of SNP Genotypes and Genetic Relatedness from DNA Methylation Data. Genom. Proteom. Bioinform. 22(3) (2024)- 2022
- [j6]Shanshan Cheng, Jingjing Lyu, Xian Shi, Kai Wang, Zengmiao Wang, Minghua Deng, Baoluo Sun, Chaolong Wang
:
Rare variant association tests for ancestry-matched case-control data based on conditional logistic regression. Briefings Bioinform. 23(2) (2022) - [j5]Qiuxuan Liu, Degang Wu, Chaolong Wang:
Identification of genomic regions distorting population structure inference in diverse continental groups. Quant. Biol. 10(3): 287 (2022) - 2021
- [j4]Jinzhuang Dou, Degang Wu, Lin Ding, Kai Wang, Minghui Jiang, Xiaoran Chai, Dermot F. Reilly, E. Shyong Tai, Jianjun Liu, Xueling Sim, Shanshan Cheng, Chaolong Wang:
Using off-target data from whole-exome sequencing to improve genotyping accuracy, association analysis and polygenic risk prediction. Briefings Bioinform. 22(3) (2021)
2010 – 2019
- 2017
- [j3]Xuefeng Wang, Zhenyu Zhang, Nathan Morris, Tianxi Cai, Seunggeun Lee, Chaolong Wang, Timothy W. Yu, Christopher A. Walsh, Xihong Lin:
Rare variant association test in family-based sequencing studies. Briefings Bioinform. 18(6): 954-961 (2017) - [j2]Daniel Taliun, Sonia P. Chothani, Sebastian Schönherr, Lukas Forer, Michael Boehnke, Gonçalo R. Abecasis, Chaolong Wang:
LASER server: ancestry tracing with genotypes or sequence reads. Bioinform. 33(13): 2056-2058 (2017) - [j1]Jin Liu, Xiang Wan, Chaolong Wang, Chao Yang, Xiaowei Zhou, Can Yang:
LLR: a latent low-rank approach to colocalizing genetic risk variants in multiple GWAS. Bioinform. 33(24): 3878-3886 (2017)
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