DIAO LAB AT DUKE
  • Home
  • Research
  • Team
  • Lab news
Yu received his PhD training from a virology lab led by Dr. Jin Zhong at Institut Pasteur of Shanghai, where he aquired solid knowledge in virology and immunology. He identified the lipid synthetase CH25H as an immune response effector, which expands the appreciation of lipid metabolism in the host antiviral immune response (Xiang et al, 2015, JVI). Yu firmly believe that modern biologists must be adept at experimentation as well as computation, then he joined Dr. Leng Han’s lab at UTHealth in 2016 for the training in bioinformatics. He has developed a computational pipeline to characterize alternative polyadenylation (APA) and revealed the important roles of APA in cancer development by analyzing The Cancer Genome Atlas (TCGA) dataset (Xiang et al., 2018, JNCI).

Yu is starting in the Diao lab as a postdoctoral fellow in Oct 2018. He will integrate his comprehensive skillsets in both experimental and computational biology to investigate the gene regulation mechanism that controls skeletal muscle regeneration and aging.


Selected Publication (*co-first author)
1.   Xiang, Y, Ye, Y, Zhang, Z, Han L. (2018) Maximizing the Utility of Cancer Transcriptomic Data. Trends Cancer
.
2. Xiang, Y., Ye, Y., Lou, Y., Yang, Y., Cai, C., Zhang, Z., Mills, T., Chen, N.-Y., Kim, Y., Muge Ozguc, F. et al. (2018) Comprehensive Characterization of Alternative Polyadenylation in Human Cancer. JNCI: Journal of the National Cancer Institute, djx223-djx223.
3. Ye, Y., Xiang, Y., Ozguc, F.M., Kim, Y., Liu, C., Park, P.K., Hu, Q., Diao, L., Lou, Y., Lin, C. et al. (2017) The genomic landscape and pharmacogenomic interactions of circadian genes in cancer chronotherapy. Cell System. Accepted.
4. Gong, J*., Li, Y*., Liu, C.-j*., Xiang, Y*., Li, C., Ye, Y., Zhang, Z., Hawke, D.H., Park, P.K., Diao, L. et al. (2017) A Pan-cancer Analysis of the Expression and Clinical Relevance of Small Nucleolar RNAs in Human Cancer. Cell Reports, 21, 1968-1981.
5. Feng, J*., Xiang, Y*., Xia, S., Liu, H., Wang, J., Ozguc, F.M., Lei, L., Kong, R., Diao, L., He, C. et al. (2017) CircView: a visualization and exploration tool for circular RNAs. Briefings in Bioinformatics, bbx070-bbx070.
6. Xiang, Y., Tang, J.J., Tao, W., Cao, X., Song, B.L. and Zhong, J. (2015) Identification of Cholesterol 25-Hydroxylase as a Novel Host Restriction Factor and a Part of the Primary Innate Immune Responses against Hepatitis C Virus Infection. J. Virol., 89, 6805-6816.
7. Lu, J., Xiang, Y., Tao, W., Li, Q., Wang, N., Gao, Y., Xiang, X., Xie, Q. and Zhong, J. (2014) A novel strategy to develop a robust infectious hepatitis C virus cell culture system directly from a clinical isolate. J. Virol., 88, 1484-1491.
8. Qi, Y*., Xiang, Y*., Wang, J., Qi, Y., Li, J., Niu, J. and Zhong, J. (2013) Inhibition of hepatitis C virus infection by polyoxometalates. Antiviral Res., 100, 392-398.
Contacts
307 Research Drive, 
373 Nanaline Duke Building, Box 3709
​
Duke University School of Medicine
Durham, NC 27710
Email: diaolab@duke.edu
Telephone: 919-684-7090
Fax: 919-684-8090
If you are a Duke CMB, DSCB, and UPGG graduate student and you are interested in gene regulation, chromatin, single-cell genomics, stem cell, regeneration, aging, cancer research, genomic methods development, bioinformatics and computational biology, please contact us to set up a rotation!
  • Home
  • Research
  • Team
  • Lab news