Dr. Xiaowei Zhan
Associate Professor of the Quantitative Biomedical Research Center in the Department of Population and Data Sciences at UT Southwestern Medical Center.
Before joining UT Southwestern, Dr. Zhan was a doctoral student in the Center of Statistical Genetics in Department of Biostatistics at the University of Michigan, a master student in the Mathematics and Statistics program at the University of Minnesota-Duluth, and a bachelor student in the department of automation at Tsinghua University, Beijing, China.
Dr. Zhan’s group focuses on statistical genetics and statistical computations. We use bioinformatics and statistical approaches to address emerging medical questions. Since 2014, our group has published more than 50 papers in human medical genetics, human microbiome, and antibiotic resistance research. For example, our group has developed Bayesian statistical models to analyze microbiome data from cancer immune checkpoint therapy patients and derived microbial biomarkers in a prediction model. All our research is accompanied with easy-to-use and efficient software package to facilitate both internal and external research communities. Please visit the publication page for more details.
Research Interests
We develop translational models to tackle complex biomedical challenges, with the goal of promoting health for all.
Human genetics
We use statistical genetics to study human complex trait diseases. This includes genetic association studies accompanied with efficient analysis software packages.
Microbiome
The human microbiome consists of both beneficial and harmful bacteria that coexist with us. We develop a series of quantitative approach to study them, mainly in the context of cancer immune checkpoint therapy patients and microbial biomarkers research.
Antibiotic resistance
Antibiotic resistance poses a global health threat. We utilize the cutting-edge sequencing technology and machine algorithms. With close collaboraiton wtih clinicians, we have been developing diagnosis tools to tackle this threat.
Deep learning
To address biomedical challenges, we develop state-of-the-art deep learning models that can solve domain-specific questions.
Software
We develop scientific software for the broad research communities.
ThunderVCF
Low-coverage genotype calling using Hidden Markov-chain Model (HMM) [Developing]
Selected Publications
For a complete list of publication, please visit PubMed
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Zhan X,Hu Y, Li B, Abecasis GR, Liu DJ. RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data. Bioinformatics (Oxford, England). 2016; 32(9):1423-6.
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Zhan X,Liu DJ. SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations. Genetic epidemiology. 2015; 39(8):619-23.
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Wang T*, Zhan X*, Bu CH*, Lyon S*, Pratt D, Hildebrand S, Choi JH, Zhang Z, Zeng M, Wang KW, Turer E, Chen Z, Zhang D, Yue T, Wang Y, Shi H, Wang J, Sun L, SoRelle J, McAlpine W, Hutchins N, Zhan X, Fina M, Gobert R, Quan J, Kreutzer M, Arnett S, Hawkins K, Leach A, Tate C, Daniel C, Reyna C, Prince L, Davis S, Purrington J, Bearden R, Weatherly J, White D, Russell J, Sun Q, Tang M, Li X, Scott L, Moresco EM, McInerney GM, Karlsson Hedestam GB, Xie Y, Beutler B. Real-time resolution of point mutations that cause phenovariance in mice. Proceedings of the National Academy of Sciences of the United States of America.2015; 112(5):E440-9.
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Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, Brooks M, Ratnapriya R, Boleda A, Grassmann F, von Strachwitz C, Olson LM, Buitendijk GH, Hofman A, van Duijn CM, Cipriani V, Moore AT, Shahid H, Jiang Y, Conley YP, Morgan DJ, Kim IK, Johnson MP, Cantsilieris S, Richardson AJ, Guymer RH, Luo H, Ouyang H, Licht C, Pluthero FG, Zhang MM, Zhang K, Baird PN, Blangero J, Klein ML, Farrer LA, DeAngelis MM, Weeks DE, Gorin MB, Yates JR, Klaver CC, Pericak-Vance MA, Haines JL, Weber BH, Wilson RK, Heckenlively JR, Chew EY, Stambolian D, Mardis ER, Swaroop A, Abecasis GR. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature genetics. 2013; 45(11):1375-9.
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Kim J, Greenberg D, Pifer R, Jiang S, Xiao G, Shelburne S, Koh A, Xie Y, Zhan X. VAMPr: VAriant Mapping and Prediction of antibiotic resistance via explainable features and machine learning. PLoS Comput Biol. 2019 February; doi: 10.1101/537381.
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Jiang S, Xiao G, Koh A, Kim J, Li Q, Zhan X. A Bayesian zero-inflated negative binomial regression model for the integrative analysis of microbiome data. Biostatistics. Dec 17; doi: 10.1093/biostatistics/kxz050.
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Jiang Y, Chen S, McGuire D, Chen F, Liu M, Iacono WG, Hewitt JK, Hokanson JE, Krauter K, Laakso M, Li KW, Lutz SM, McGue M, Pandit A, Zajac GJM, Boehnke M, Abecasis GR, Vrieze SI, Zhan X*, Jiang B*, Liu DJ*. Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes. PLoS genetics. 2018; 14(7):e1007452.
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Kim J, Kim MS, Koh AY, Xie Y, Zhan X. FMAP: Functional Mapping and Analysis Pipeline for metagenomics and metatranscriptomics studies. BMC bioinformatics. 2016; 17(1):420.
Our Team
My lab members includes doctoral students, staff members, and adminitration support members. We shared resources with the Quantitative Biomedical Research Center. We also collaborate closely within UT Southwestern campus and worldwide. We are active in seeking potential doctoral students, post-docs, and staff members
Jiwoong Kim
Computational BiologistWen Fan
Doctoral studentArt Taychameekiatchai
Doctoral studentShuheng Gan
Computational BiologistSuzette Palmer
Doctoral StudentRuheng Wang
Doctoral StudentJonathan Wang
Intern StudentZiyun Zhou
Visiting ScholarShuang Jiang
AlumniYiqing Wang
AlumniSen Yang
AlumniContact
Location
5323 Harry Hines Blvd.
Ste. H9.124
Dallas, TX 75390-8821
Xiaowei.Zhan@UTSouthwestern.edu
Office
+1 (214) 648-5194
Fax
+1 (214) 648-1663