Lin Xu, Ph.D. Titles and Appointments Assistant Professor School Graduate School Department Public Health | Pediatrics Graduate Programs Biomedical Engineering Biography With a Ph.D. in Biostatistics and Bioinformatics from Cornell University, I have developed expertise in the integrated analysis of high-dimensional datasets, deep learning, Bayesian modeling, and bioinformatics algorithms, as well as designing clinical studies for both the analytic and clinical validation of biomarkers. During my postdoctoral training, I expanded my expertise by bridging biostatistical methodologies with clinical applications, particularly in translating biomarker discoveries into validated clinical tools. Currently, as a tenure-track Assistant Professor at UT Southwestern, my research centers on developing and applying deep learning, Bayesian statistical models, and bioinformatics tools to identify and validate robust disease-specific biomarkers and disease genes, uncover new therapeutic targets and treatment strategies, and build software platforms and web portals for accessible data analysis and sharing. Since establishing my laboratory at UT Southwestern in 2022, I have published 94 peer-reviewed research articles, with 21 as co- or corresponding author. My lab has published a series of deep learning and statistics algorithms to identify clinical biomarkers and disease genes from bulk, single-cell, and spatially resolved omics data, advancing biological and translational insights across cancer, heart, brain, and muscle biology. Among these publications, I served as co-/corresponding authors to develop iExCN 2.0 algorithm for bulk multiomics data integration (Xu et al. Nature Communications, 2023; impact factor (IF) 14.7), ilMPACT algorithm for spatial transcriptomics analysis (Jiang et al. Genome Biology, 2024; IF: 17.9), EpiTR framework for transcriptional factor identification and analysis (Lu et al. Briefings in Bioinformatics, 2024, IF: 14.0), BayeSMART algorithm for multi-sample spatial omics analysis (Guo et al. Briefings in Bioinformatics, 2024), COSMOS algorithm for spatially resolved multi-omics data integration (Zhou et al. Nature Communications, 2025), SpaSNE algorithm for spatially guided dimension reduction (Zhou et al. GigaScience, 2025; IF: 11.8), and BIT algorithm for epigenomics-based transcriptional factor analysis (Lu et al. Nature Communications, 2025). These algorithms and computational frameworks have been applied in our recent studies published in Nature (Huang et al. 2020, and Engreitz JM, et al. 2025), Cell (Wei et al. 2023), Science (Lebak et al. 2023), Nature Medicine (Cai et al. 2023), Nature Machine Intelligence (Lu et al. 2022), Nature Immunology (Yang et al. 2025), Circulation (Lebak et al. 2023, Bann et al. 2025, and Ding et al. 2025, IF: 38.6), Cancer Cell (Shi et al. 2022, and Zhu et al. 2023; IF: 44.5), and many others. More importantly, my laboratory pioneers the application of artificial intelligence (AI) —particularly foundation models and large language models (LLMs)—to drive biological and medical discovery. Our work focuses on developing interpretable and generalizable AI frameworks that extend the capabilities of foundation models beyond text and vision into genomics and precision medicine. As a major milestone, one of our recently developed AI algorithms for clinical diagnosis prediction was invited for an oral presentation at the Association for the Advancement of Artificial Intelligence (AAAI) Conference —one of the oldest and most impactful international conferences in the artificial intelligence field. Founded in 1980, the AAAI Conference is widely recognized as a flagship venue for foundational and cutting-edge advances across the entire spectrum of artificial intelligence—spanning machine learning, reasoning, robotics, and AI for science—and is ranked among the top three AI conferences globally by Google Scholar Metrics. Among fewer than 40 biology-oriented AI studies featured annually, this recognition underscores the novelty and cross-disciplinary impact of my research and reflects my research team’s commitment to bridging AI and biomedical science. Since I joined UT Southwestern as a tenure-track Assistant Professor, my lab has developed multiple deep learning models and statistics algorithms to identify new disease genes and therapeutic targets [e.g., Huang et al. Nature (2020), Lu et al. Nature Machine Intelligence (2022), Chai et al. Nature Medicine (2022), Takahiko et al. Science Translational Medicine (2022) (Cover Story), Shi et al. Cancer Cell (2022), Lebek et al. Science (2023), Xu et al. Nature Communications (2023), Zhu et al. Cancer Cell (2023), Zhang et al. Journal of Clinical Investigation (2023), He et al. Nature Communications (2023), Yu et al. Nature Communications (2023), Santos et al. Nature Communications (2023), Li et al. Nature Communications (2023), Wei et al. Cell (2023), Hernandez et al. PNAS (2024), Hu L et al. Mol Cell (2024), Eglenen-Polat et al. Nature Communications (2024), Lin CC et al. Nature Communications (2024), Xu L. et al. Nature Communications (2024), Venkateswaran N. et al. Nature Communications (2024), Chen S. et al. Nature Communications (2025), Liao C, Nature Communications (2025), Yang X. et al. Nature Immunology (2025), Lu ZY. et al. Nature Communications (2025), Zhou Y. et al. Nature Communications (2025), Adachi Y et al. J Clin Invest. (2025), Napolitano F, et al. J Clin Invest. (2025), Bann et al. Circulation (2025), Ding et al. Circulation (2025), Caravia XM, et al. Proc. Natl. Acad. Sci. (2025), Guan P, et al. Proc. Natl. Acad. Sci. (2025), Engreitz JM, et al. Nature (2025)]. Since 2021, my lab’s research has been published in a series of high-impact journals, including Nature, Science, Cell, Nature Medicine, Cancer Cell, Elife, PNAS, Nature Machine Intelligence, Nature Immunology, Nature Metabolism, Nature Communications, Science Translational Medicine, Science Advance, Molecular Cell, Genes & Development, Cell Reports, Journal of Clinical Investigation, Circulation, Circulation Research, and Developmental Cell. Research Interest AI agent, LLM, deep learning, multi-omics, single-cell and spatial omics, epigenomics Publications Featured Publications Dynamic Transcriptional Responses to Injury of Regenerative and Non-regenerative Cardiomyocytes Revealed by Single-Nucleus RNA Sequencing. Cui M, Wang Z, Chen K, Shah AM, Tan W, Duan L, Sanchez-Ortiz E, Li H, Xu L, Liu N, Bassel-Duby R, Olson EN, Dev. Cell 2020 Mar Twist2 amplification in rhabdomyosarcoma represses myogenesis and promotes oncogenesis by redirecting MyoD DNA binding. Li S, Chen K, Zhang Y, Barnes SD, Jaichander P, Zheng Y, Hassan M, Malladi VS, Skapek SX, Xu L, Bassel-Duby R, Olson EN, Liu N, Genes Dev. 2019 Apr SR-B1 drives endothelial cell LDL transcytosis via DOCK4 to promote atherosclerosis. Huang L, Chambliss KL, Gao X, Yuhanna IS, Behling-Kelly E, Bergaya S, Ahmed M, Michaely P, Luby-Phelps K, Darehshouri A, Xu L, Fisher EA, Ge WP, Mineo C, Shaul PW, Nature 2019 Apr DIGREM: an integrated web-based platform for detecting effective multi-drug combinations. Zhang M, Lee S, Yao B, Xiao G, Xu L, Xie Y Bioinformatics 2018 Oct Integrative Bayesian Analysis Identifies Rhabdomyosarcoma Disease Genes. Xu L, Zheng Y, Liu J, Rakheja D, Singleterry S, Laetsch TW, Shern JF, Khan J, Triche TJ, Hawkins DS, Amatruda JF, Skapek SX Cell Rep 2018 Jul 24 1 238-251 as a mediator of rhabdomyosarcoma tumorigenesis. Kendall GC, Watson S, Xu L, LaVigne CA, Murchison W, Rakheja D, Skapek SX, Tirode F, Delattre O, Amatruda JF Elife 2018 Jun 7 Dynamic epistasis for different alleles of the same gene. Xu L, Barker B, Gu Z, Proc. Natl. Acad. Sci. U.S.A. 2012 Jun 109 26 10420-5 Genetic architecture of growth traits revealed by global epistatic interactions. Xu L, Jiang H, Chen H, Gu Z, Genome Biol Evol 2011 3 909-14 Targeting kinesin family member 20A sensitizes stem-like triple-negative breast cancer cells to standard chemotherapy. Adachi Y, Chen W, Zhang C, Wang T, Gildor N, Shi R, Fu H, Takeda M, Liang Q, Zhao F, Liu H, Fang J, Zhou J, Yao H, Hu L, Li S, Guo L, Xu L, Xie L, Chen X, Liao C, Zhang Q, J Clin Invest 2025 Dec 135 24 CD8+ T cells in the tumor microenvironment modulate response to endocrine therapy in breast cancer. Napolitano F, Wang Y, Sudhan DR, Gonzalez-Ericsson PI, Formisano L, Unni N, Shakeel S, Zhu JZ, Ahuja K, Guo L, Chica-Parrado MR, Matsunaga Y, Luna P, Lin CA, Uemoto Y, Lee KM, Ma H, Evans NJ, Servetto A, Mendiratta S, Barnes SD, Bianco R, Fang YV, Xu L, Lee J, Wang T, Balko JM, Mills GB, Labrie M, Hanker AB, Arteaga CL, J Clin Invest 2025 Dec Results 1-10 of 43 1 2 3 4 5 Next Last Honors & Awards Hyundai Hope Scholar from Hyundai Hope on Wheels Foundation (2024) Sam Day Research Scholar from Sam Day Foundation (2024) Independent Investigator Research Award from Rally Foundation (2020) Career Development Award from Childrens Cancer Fund (2018) Professional Associations/Affiliations Department of Pediatrics (2021) Quantitative Biomedical Research Center, Peter ODonnell Jr. School of Public Health (2021)