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研究员

 

贾佩林 ( JIA Peilin )

职    称:
研究员
职    务:
 
E-Mail:
pjia@big.ac.cn
学科类别:
生物信息学 基因组学 遗传学
 
 
 
 学习经历:
 

1999年9月-2003年7月 大连理工大学,生物工程专业,学士学位

2003年9月-2008年7月 中科院上海生命科学研究院,生物信息专业,博士学位


 工作经历:
 

2008年9月-2009年6月 Virginia CommonWealth University,postdoc

2009年7月-2016年2月 Vanderbilt University,postdoc (2009.7-2012.6),research-track assistant professor (2012.7-2016.2)

2016年3月-2020年10月 The University of Texas Health Science Center at Houston,tenure-track assistant professor


 主要研究领域:
 

1.精准健康:人类复杂疾病的遗传学研究。我们致力于解析与疾病相关的遗传学基础和功能研究,关注致病基因及genetic variants。主要利用统计学、数学和数据挖掘的知识,开发生物信息学的算法与工具以研究疾病的致病机理。

2.精准健康:癌症组学研究。我们致力于开发前沿的算法以检测driver mutations,探讨癌症成因,癌症基因的致病原理和在细胞中的影响,及开发深度学习算法以预测个性化的治疗方案。

3.脑相关疾病研究。我们关注三类脑相关疾病:精神类疾病,退行性疾病和认知相关疾病。开发及使用计算方法以分析和整合多组学数据,深入研究疾病的遗传学基础和疾病的相关性。


 承担科研项目情况:
 

 代表论著:
 

1. Pei G, Hu R, Dai Y, Manuel AM, Zhao Z*, Jia P* (accepted) Predicting regulatory variants using a dense epigenomic mapped CNN model elucidated the molecular basis of trait-tissue associations. Nucleic Acids Research

 

2. Dai Y, Hu R, Manuel AM, Liu A, Jia P*, Zhao Z* (accepted) CSEA-DB: An omnibus for human complex trait and cell type associations. Nucleic Acids Research

 

3. Pei G, Hu R, Dai Y, Zhao Z*, Jia P* (2020) Decoding whole-genome mutational signatures in 37 human pan-cancers by denoising sparse autoencoder neural network. Oncogene 39:5031-5041. PMCID: PMC7334101

 

4. Jia P, Dai Y, Hu R, Pei G, Manuel A, Zhao Z (2020) TSEA-DB: A trait-tissue association map for human complex traits and diseases. Nucleic Acids Research 48(D1):D1022-D1030

 

5. Jia P, Pei G, Zhao Z (2019) CNet: A multi-omics approach to detecting clinically associated, combinatory genomic signatures. Bioinformatics 35(24):5207-5215

 

6. Pei G, Dai, Y, Zhao Z*, Jia P* (2019) deTS: tissue-specific enrichment analysis to decode tissue specificity. Bioinformatics 35(19):3842-3845

 

7. Huang Y, Wang J, Jia P, Li X, Pei G, Wang C, Fang X, Zhao Z, Cai Z, Yi X, Wu S, Zhang B (2019) Clonal architectures predict clinical outcome in clear cell renal cell carcinoma. Nature Communications 10(1):1245

 

8. Jia P, Zhao Z (2019) Characterization of tumor-suppressor gene inactivation events in 33 cancer types. Cell Reports 26:496-506

 

9. Jia P, Chen X, Xie W, Kendler KS, Zhao Z (2019) Mega-analysis of Odds Ratio (MegaOR): A convergent method for deep understanding the genetic evidence in schizophrenia. Schizophrenia Bulletin 45(3), 698-708

 

10. Jia P, Chen X, Fanous AH, Zhao Z (2018) Convergent roles of de novo mutations and common variants in schizophrenia in tissue-specific and spatiotemporal co-expression network. Translational Psychiatry 8(1):105

 

11. Jia P, Zhao Z (2016) Impacts of somatic mutations on gene expression: an association perspective. Briefings in Bioinformatics 18(3):413-425

 

12. Jia P, Han G, Zhao J, Lu P, Zhao Z (2017) SZGR2.0: a one-stop shop of schizophrenia-associated genes. Nucleic Acids Research 45(D1):D915-D924

 

13. Jia P, Zhao Z, Hulgan T, Bush W, Samuels DC, Bloss C, Heaton R, Ellis R, Schork N, Marra C, Collier AC, Clifford D, Gelman B, Sacktor N, Morgello S, Simpson D, McCutchan JA, Letendre S, Barnholtz-Sloan J, Franklin DR, and Grant I for the CHARTER Study Group, Kallianpur, AR (2017) Genome-wide association study of HIV-Associated Neurocognitive Disorder (HAND): a CHARTER Group Study. American Journal of Medical Genetics, 174(4):413-426

 

14. McGirt LY#, Jia P#, Baerenwald DA, Dahlman K, Zic JA, Zwerner JP, Hucks D, Dave U, Zhao Z, Eischen CM (2015) Whole genome analysis reveals oncogenic alterations in mycosis fungoides. Blood 126(4): 508-519

 

15. Wang Q, Yu H, Zhao Z*, Jia P* (2015) EW_dmGWAS: Edge-Weighted dense module search for genome-wide association studies and gene expression profiles. Bioinformatics, 31, 2591-2594

 

16. Jia P, Wang Q, Chen Q, Hutchinson K, Pao W, Zhao Z (2014) MSEA: detection and quantification of mutation hotspots through mutation set enrichment analysis. Genome Biology 15:489 (editors'pick)

 

17. Jia P, Jin H, Meador CB, Xia J, Ohashi K, Liu L, Pirazzoli V, Dahlman KB, Politi K, Michor F, Zhao Z, Pao W (2013) Next-generation sequencing of paired tyrosine kinase inhibitor-sensitive and -resistant EGFR mutant lung cancer cell lines identifies spectrum of DNA changes associated with drug resistance. Genome Research 23:1434-1445

 

18. Jia P, Wang L, Fanous, AH, Pato CN, Edwards TL, The International Schizophrenia Consortium, Zhao Z (2012) Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. PLoS Computational Biology 8(7): e1002587

 

19. Jia P#, Zheng S#, Long J, Zheng W, Zhao Z (2011) dmGWAS: dense module searching for genome-wide association studies in protein-protein interaction networks. Bioinformatics. 27(1) 95-102

 

20. Jia P, Sun J, Guo AY, Zhao Z (2010) SZGR: A comprehensive schizophrenia gene resource. Molecular Psychiatry 15:453-462


 社会任职:
 

 获奖及荣誉:
 

2011 2010 NARSAD Young Investigator Award (2011-2013), National Alliance for Research on Schizophrenia and Depression

2011 Finalist, the 2010/2011 Vanderbilt Postdoc of the Year Award