The objective of this Core is to assist CEG investigators in converting the genomic and protein data intomeaningful information (knowledge) through the use of appropriate statistical methods and computational tools.The Bioinformatics F&S Core has three specific aims.[1] The first aim is to assist CEG researchers in designing and analyzing gene-expressionexperiments. This will encompass consulting researchers on the relative importance of different types ofexperimental replicates, choosing the appropriate experimental design, managing and assessing the quality ofthe obtained data, identifying differentially expressed genes using appropriate statistical analysis, identifyingsignificant patterns of expression through the clustering of expression data, and correlating differentiallyexpressed or co-expressed groups of genes with information about affected pathways, genomic location, andstructure of involved genes and other biologically relevant information. In addition to using the best of currentlyavailable methods, Core members will develop new methods for identifying differentially expressed genesusing the empirical Bayesian framework end explicit models relating variability of gene-expressionmeasurements and the level of gene expression.[2] The second aim is to assist CEG investigators in evaluating their experimental data in the contextof other relevant expression experiments and types of biologically relevant data available. In thisrespect, the Bioinformatics F&S Core will maintain the database of all gene-expression experimentsperformed by CEG members and develop a web server to facilitate access to relevant internally and externallygenerated gene-expression data. Using in-house developed statistical models, Core members will developprotocols for integrative analysis of diverse microarray datasets and use them to analyze accumulated CEGmicroarray data. Results of such analyses will incorporate structure-based functional annotations of impliedinteractions, and access to the results of the analysis will be facilitated through appropriate web-basedapplications.[3] The third aim is to assist CEG investigators with the management and analysis of data generatedby other genomic and proteomic technologies. Core members will assist with non-expression microarraytechnologies such as GeneChip-based SNP-genotyping, assessing transcription factor binding sites ('ChlP-on-Chip'), MicroRNA (miRNA) profiles, and CpG Island profiles, which are being introduced in the general offeringof the Genomics Core. Core members will also assist with optimal use of different tools for mass peptidefingerprinting, mass spectrometric protein profiling, and any other proteomic assay that might become availableover the next funding period. The Core will accumulate peptide mass spectra from CEG researchers anddevelop novel machine learning algorithms for mass peptide fingerprinting.The Core includes experts in data management, statistical analysis, machine learning, microarray dataanalysis, proteomics, sequence analysis, and protein structure modeling. To fulfill specific aims, the Core willutilize state-of-the-art data-management solutions that will facilitate the tracking of all relevant aspects ofexperimental data and integration of data across different experiments, experimental platforms, and modelorganisms. Core members will use the most up-to-date analytical approaches and develop new methods foridentifying reproducible differences and similarities in behavior of different biological entities within a singleexperiment or across multiple databases, platforms, model organisms, and ultimately different data types.Finally, Core members will use appropriate technologies for facilitating web-based access, analysis and miningof experimental data, and analytical results.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
2P30ES006096-16A1
Application #
7548881
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
16
Fiscal Year
2008
Total Cost
$208,123
Indirect Cost
Name
University of Cincinnati
Department
Type
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Bermúdez, Mei-Ling; Skelton, Matthew R; Genter, Mary Beth (2018) Intranasal carnosine attenuates transcriptomic alterations and improves mitochondrial function in the Thy1-aSyn mouse model of Parkinson's disease. Mol Genet Metab 125:305-313
Reigle, Beverly S; Zhang, Bin (2018) Women's Rehabilitation Experiences Following Breast Cancer Surgery. Rehabil Nurs 43:195-200
Whitt, Jordan; Woo, Vivienne; Lee, Patrick et al. (2018) Disruption of Epithelial HDAC3 in Intestine Prevents Diet-Induced Obesity in Mice. Gastroenterology 155:501-513
Uno, Shigeyuki; Nebert, Daniel W; Makishima, Makoto (2018) Cytochrome P450 1A1 (CYP1A1) protects against nonalcoholic fatty liver disease caused by Western diet containing benzo[a]pyrene in mice. Food Chem Toxicol 113:73-82
Vuong, Ann M; Yolton, Kimberly; Poston, Kendra L et al. (2018) Childhood polybrominated diphenyl ether (PBDE) exposure and executive function in children in the HOME Study. Int J Hyg Environ Health 221:87-94
Lee, Alison G; Le Grand, Blake; Hsu, Hsiao-Hsien Leon et al. (2018) Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects. Respir Res 19:76
Leung, Yuet-Kin; Ouyang, Bin; Niu, Liang et al. (2018) Identification of sex-specific DNA methylation changes driven by specific chemicals in cord blood in a Faroese birth cohort. Epigenetics 13:290-300
Kim, Stephani; Xu, Xijin; Zhang, Yuling et al. (2018) Metal concentrations in pregnant women and neonates from informal electronic waste recycling. J Expo Sci Environ Epidemiol :
Chen, Jing; Gálvez-Peralta, Marina; Zhang, Xiang et al. (2018) In utero gene expression in the Slc39a8(neo/neo) knockdown mouse. Sci Rep 8:10703
Abdel-Hameed, Enass A; Rouster, Susan D; Boyce, Ceejay L et al. (2018) Ultra-Deep Genomic Sequencing of HCV NS5A Resistance-Associated Substitutions in HCV/HIV Coinfected Patients. Dig Dis Sci 63:645-652

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