With the advance of genomic technologies including microarray and next generation sequencing (NGS) in recent years, a vast amount of genomic data has been generated. The quality control, statistical analysis and integration/interpretation of multi-dimensional large-scale data are facing new challenges. Bioinformatics, a interdisciplinary field that involves computer science, statistics and biology, is playing pivotal roles in genomic data analysis and integration in biomedical research. The major goals of Bioinformatics Core are 1) to promote the understanding the genomics and molecular mechanism of HIV-associated kidney diseases in human or mouse models and 2) to facilitate the interaction and data sharing among internal and external collaborators. To achieve these goals, we propose the following specific aims: 1) we will provide bioinformatic data analysis on high throughput deep-sequencing/microarray experiments to PPG projects ad statistical analysis to pathology and clinical core. We will be responsible for experimental design, data quality control, statistic and system biology analysis/interpretation of sequence data, transcriptomic and epigenomic profiles using next generation sequencing or microarray technologies; We will be fully engaged in each PPG project/research core that needs bioinformatics support and closely work with researchers and PI on any aspect related to bioinformatics/statistics. 2) We will implement a web-based data portal for data sharing among both internal and external investigators. We will develop a MIAME-compliant centralized database for storage of genomic and phenotypic/ pathological/clinical data from PPG project/core and a user-friendly interface for data query and online visualization; we will also integrate the data portal with LINCS-BD2K system for systematic data analysis to identify potential drug targets. 3) We will develop novel pipelines to facilitate analysis and integration of diverse genomic data from HIV virus and the host and meta-analysis of multiple datasets generated from PPG projects and relevant public datasets. We will identify meta signatures across multiple datasets and meta co-regulated network for better understanding of gene regulation associated with HIV- associated kidney diseases.

Public Health Relevance

Bioinformatics Core will provide state of art bioinformatics services that will promote the genomic study of HIV- associated kidney diseases and facilitate the interaction and data sharing among the internal and external collaborators. Bioinformatics core will provide genomic data analysis to PPG projects and statistical analysis to pathological/clinical cores and will also develop a web-based portal for data integration and sharing among collaborators.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
2P01DK056492-17A1
Application #
9204212
Study Section
Special Emphasis Panel (ZDK1-GRB-1 (M6)P)
Project Start
Project End
Budget Start
2016-08-01
Budget End
2017-07-31
Support Year
17
Fiscal Year
2017
Total Cost
$163,803
Indirect Cost
$17,899
Name
Baylor College of Medicine
Department
Type
Domestic Higher Education
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Chan, Lili; Asriel, Benjamin; Eaton, Ellen F et al. (2018) Potential kidney toxicity from the antiviral drug tenofovir: new indications, new formulations, and a new prodrug. Curr Opin Nephrol Hypertens 27:102-112
Swanepoel, Charles R; Atta, Mohamed G; D'Agati, Vivette D et al. (2018) Kidney disease in the setting of HIV infection: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int 93:545-559
Zhong, Fang; Chen, Zhaohong; Zhang, Liwen et al. (2018) Tyro3 is a podocyte protective factor in glomerular disease. JCI Insight 3:
Palau, Laura; Menez, Steven; Rodriguez-Sanchez, Javier et al. (2018) HIV-associated nephropathy: links, risks and management. HIV AIDS (Auckl) 10:73-81
Zhong, Fang; Chen, Haibing; Xie, Yifan et al. (2018) Protein S Protects against Podocyte Injury in Diabetic Nephropathy. J Am Soc Nephrol 29:1397-1410
Hong, Quan; Zhang, Lu; Das, Bhaskar et al. (2018) Increased podocyte Sirtuin-1 function attenuates diabetic kidney injury. Kidney Int 93:1330-1343
Fu, Jia; Wei, Chengguo; Zhang, Weijia et al. (2018) Gene expression profiles of glomerular endothelial cells support their role in the glomerulopathy of diabetic mice. Kidney Int 94:326-345
Corona-Villalobos, Celia P; Shlipak, Michael G; Tin, Adrienne et al. (2017) Predictors of Acute Renal Injury Study (PARIS) among HIV-positive individuals: design and methods. BMC Nephrol 18:289
Gu, Xiangchen; Mallipattu, Sandeep K; Guo, Yiqing et al. (2017) The loss of Krüppel-like factor 15 in Foxd1+ stromal cells exacerbates kidney fibrosis. Kidney Int 92:1178-1193
Wei, Chengguo; Li, Li; Menon, Madhav C et al. (2017) Genomic Analysis of Kidney Allograft Injury Identifies Hematopoietic Cell Kinase as a Key Driver of Renal Fibrosis. J Am Soc Nephrol 28:1385-1393

Showing the most recent 10 out of 111 publications