The importance of analyzing large data sets (e.g., RNAseq, ChIP-seq, genomic studies, etc) are increasingly used for a global analysis of molecular changes with age or with aging interventions. However, access to the bioinformatics and statistical expertise necessary to analyze and interpret these data can be rate-limiting for many investigators, especially junior investigators. Additionally, in the age of Big Data, there is a need to focus the development of bioinformatics methods that will help investigators answer aging-related questions. The goal of the GeroInformatics Core is to assist investigators in Oklahoma City and throughout the nation with bioinformatics and statistical analyses specifically designed for investigators studying aging questions. The Core will accomplish this goal using established bioinformatic methods for data analysis, statistical support for experimental design and analysis, as well as using novel and innovative approaches for data analysis developed by the GeroInformatics Core, specifically designed to analyze aging data bases. The GeroInformatics Core consists of established experts in bioinformatics methods development, statistics, and the molecular biology of aging. Besides established approaches for data analysis, the GeroInformatics Core has developed bioinformatics methods to interrogate large-scale data from different perspectives, such as literature-based networks of related entities (e.g., genes, diseases, metabolites, concepts), transcriptional correlations compiled from public data sources to compare new experiments against, and annotations of genomic regions to search for experimental commonalities. Because of the growing interest in the use of single-cell RNA-sequencing to study the effect of aging on individual cells from cell cultures or tissues and because of the lack of methods to critically analyze single-cell transcriptomic data, a new function of the GeroInformatics Core in this application is to develop methods to iteratively analyze single-cell transcriptomic data and make these novel analyses available to the aging community.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
2P30AG050911-06
Application #
10044528
Study Section
Special Emphasis Panel (ZAG1)
Project Start
2015-07-15
Project End
2025-05-31
Budget Start
2020-09-01
Budget End
2021-05-31
Support Year
6
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Oklahoma Health Sciences Center
Department
Type
DUNS #
878648294
City
Oklahoma City
State
OK
Country
United States
Zip Code
73104
Schafer, Christopher; Young, Zachary T; Makarewich, Catherine A et al. (2018) Coenzyme A-mediated degradation of pyruvate dehydrogenase kinase 4 promotes cardiac metabolic flexibility after high-fat feeding in mice. J Biol Chem 293:6915-6924
Van Skike, Candice E; Jahrling, Jordan B; Olson, Angela B et al. (2018) Inhibition of mTOR protects the blood-brain barrier in models of Alzheimer's disease and vascular cognitive impairment. Am J Physiol Heart Circ Physiol 314:H693-H703
Logan, Sreemathi; Pharaoh, Gavin A; Marlin, M Caleb et al. (2018) Insulin-like growth factor receptor signaling regulates working memory, mitochondrial metabolism, and amyloid-? uptake in astrocytes. Mol Metab 9:141-155
Hadad, Niran; Unnikrishnan, Archana; Jackson, Jordan A et al. (2018) Caloric restriction mitigates age-associated hippocampal differential CG and non-CG methylation. Neurobiol Aging 67:53-66
Donovan, Elise L; Lopes, Erika Barboza Prado; Batushansky, Albert et al. (2018) Independent effects of dietary fat and sucrose content on chondrocyte metabolism and osteoarthritis pathology in mice. Dis Model Mech 11:
Ahn, Bumsoo; Pharaoh, Gavin; Premkumar, Pavithra et al. (2018) Nrf2 deficiency exacerbates age-related contractile dysfunction and loss of skeletal muscle mass. Redox Biol 17:47-58
Snider, Timothy A; Richardson, Arlan; Stoner, Julie A et al. (2018) The Geropathology Grading Platform demonstrates that mice null for Cu/Zn-superoxide dismutase show accelerated biological aging. Geroscience 40:97-103
Fulop, Gabor A; Kiss, Tamas; Tarantini, Stefano et al. (2018) Nrf2 deficiency in aged mice exacerbates cellular senescence promoting cerebrovascular inflammation. Geroscience 40:513-521
Fu, Zhongjie; Löfqvist, Chatarina A; Liegl, Raffael et al. (2018) Photoreceptor glucose metabolism determines normal retinal vascular growth. EMBO Mol Med 10:76-90
Li, Xiaomeng; Oh, Sangphil; Song, Hoogeun et al. (2018) A potential common role of the Jumonji C domain-containing 1A histone demethylase and chromatin remodeler ATRX in promoting colon cancer. Oncol Lett 16:6652-6662

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