The objective of this Core is to assist CEG investigators in converting the genomic and protein data into meaningful 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-expression experiments. This will encompass consulting researchers on the relative importance of different types of experimental replicates, choosing the appropriate experimental design, managing and assessing the quality of the obtained data, identifying differentially expressed genes using appropriate statistical analysis, identifying significant patterns of expression through the clustering of expression data, and correlating differentially expressed or co-expressed groups of genes with information about affected pathways, genomic location, and structure of involved genes and other biologically relevant information. In addition to using the best of currently available methods, Core members will develop new methods for identifying differentially expressed genes using the empirical Bayesian framework end explicit models relating variability of gene-expression measurements and the level of gene expression. [2] The second aim is to assist CEG investigators in evaluating their experimental data in the context of other relevant expression experiments and types of biologically relevant data available. In this respect, the Bioinformatics F&S Core will maintain the database of all gene-expression experiments performed by CEG members and develop a web server to facilitate access to relevant internally and externally generated gene-expression data. Using in-house developed statistical models, Core members will develop protocols for integrative analysis of diverse microarray datasets and use them to analyze accumulated CEG microarray data. Results of such analyses will incorporate structure-based functional annotations of implied interactions, and access to the results of the analysis will be facilitated through appropriate web-based applications. [3] The third aim is to assist CEG investigators with the management and analysis of data generated by other genomic and proteomic technologies. Core members will assist with non-expression microarray technologies 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 offering of the Genomics Core. Core members will also assist with optimal use of different tools for mass peptide fingerprinting, mass spectrometric protein profiling, and any other proteomic assay that might become available over the next funding period. The Core will accumulate peptide mass spectra from CEG researchers and develop novel machine learning algorithms for mass peptide fingerprinting. The Core includes experts in data management, statistical analysis, machine learning, microarray data analysis, proteomics, sequence analysis, and protein structure modeling. To fulfill specific aims, the Core will utilize state-of-the-art data-management solutions that will facilitate the tracking of all relevant aspects of experimental data and integration of data across different experiments, experimental platforms, and model organisms. Core members will use the most up-to-date analytical approaches and develop new methods for identifying reproducible differences and similarities in behavior of different biological entities within a single experiment 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 mining of 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 #
5P30ES006096-18
Application #
8054345
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2010-04-01
Budget End
2011-03-31
Support Year
18
Fiscal Year
2010
Total Cost
$185,317
Indirect Cost
Name
University of Cincinnati
Department
Type
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
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
Dobraca, Dina; Lum, Raymond; Sjödin, Andreas et al. (2018) Urinary biomarkers of polycyclic aromatic hydrocarbons in pre- and peri-pubertal girls in Northern California: Predictors of exposure and temporal variability. Environ Res 165:46-54
Miller, Marian L; Porollo, Aleksey; Wert, Susan (2018) Ultrastructure of Highly Ordered Granules in Alveolar Type II Cells in Several Species. Anat Rec (Hoboken) :
Ren, Sheng; Haynes, Erin; Hall, Eric et al. (2018) Periconception Exposure to Air Pollution and Risk of Congenital Malformations. J Pediatr 193:76-84.e6
Bhattacharya, Sukanta S; Yadav, Jagjit S (2018) Microbial P450 Enzymes in Bioremediation and Drug Discovery: Emerging Potentials and Challenges. Curr Protein Pept Sci 19:75-86
VonHandorf, Andrew; Sánchez-Martín, Francisco Javier; Biesiada, Jacek et al. (2018) Chromium disrupts chromatin organization and CTCF access to its cognate sites in promoters of differentially expressed genes. Epigenetics 13:363-375
Giannini, Courtney M; Herrick, Robert L; Buckholz, Jeanette M et al. (2018) Comprehension and perceptions of study participants upon receiving perfluoroalkyl substance exposure biomarker results. Int J Hyg Environ Health 221:1040-1046
Haque, Sulsal-Ul; Niu, Liang; Kuhnell, Damaris et al. (2018) Differential expression and prognostic value of long non-coding RNA in HPV-negative head and neck squamous cell carcinoma. Head Neck 40:1555-1564

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