My Publications
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1000 Genomes Project Consortium. 2012. “An integrated map of genetic variation from 1,092 human genomes.” Nature 135 (V): 0–9. https://doi.org/10.1038/nature11632.
Jaspal S. Kooner, Danish Saleheen, Xueling Sim, Joban Sehmi, Weihua Zhang, Philippe Frossard, Latonya F. Been, et al. 2011. “Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.” Nature Genetics. https://doi.org/10.1038/ng.921.
Yingrui Li, Hancheng Zheng, Ruibang Luo, Honglong Wu, Hongmei Zhu, Ruiqiang Li, Hongzhi Cao, et al. 2011. “Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.” Nature Biotechnology 29 (8). Nature Publishing Group: 723–30. https://doi.org/10.1038/nbt.1904.
Anubha Mahajan, Min Jin Go, Weihua Zhang, Jennifer E. Below, Kyle J. Gaulton, Teresa Ferreira, Momoko Horikoshi, et al. 2014. “Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.” Nature Genetics. https://doi.org/10.1038/ng.2897.
Oleg Mayba, Florian Gnad, Michael Peyton, Fan Zhang, Kimberly Walter, Pan Du, Melanie A Huntley, et al. 2014. “Integrative analysis of two cell lines derived from a non-small-lung cancer patient–a panomics approach.” Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing. https://doi.org/10.1109/RSETE.2011.5966134.
Keiichiro Suzuki, Chang Yu, Jing Qu, Mo Li, Xiaotian Yao, Tingting Yuan, April Goebl, et al. 2014. “Targeted Gene Correction Minimally Impacts Whole-Genome Mutational Load in Human-Disease-Specific Induced Pluripotent Stem Cell Clones.” Cell Stem Cell. https://doi.org/10.1016/j.stem.2014.06.016.
Chang Yu, Jun Yu, Xiaotian Yao, William K.K. Wu, Youyong Lu, Senwei Tang, Xiangchun Li, et al. 2014. “Discovery of biclonal origin and a novel oncogene SLC12A5 in colon cancer by single-cell sequencing.” Cell Research. https://doi.org/10.1038/cr.2014.43.
Fan Zhang, Ruoyan Chen, Dongbing Liu, Xiaotian Yao, Guoqing Li, Yabin Jin, Chang Yu, Yingrui Li, and Lachlan J M Coin. 2013. “YHap: a population model for probabilistic assignment of Y haplogroups from re-sequencing data.” BMC Bioinformatics 14: 331. https://doi.org/10.1186/1471-2105-14-331.
Fan Zhang, Matthew Flickinger, Sarah A. Gagliano Taliun, Gonçalo R. Abecasis, Laura J. Scott, Steven A. McCaroll, Carlos N. Pato, Michael Boehnke, and Hyun Min Kang. 2020. “Ancestry-agnostic estimation of DNA sample contamination from sequence reads.” Genome Research, 1–42. https://doi.org/10.1101/gr.246934.118.