The Biostatistics and Modeling Core provides a centralized plan for experimental design, data integration and predictive modeling of research data that is utilized by all of our Research Projects and Cores. We have created a multi-disciplinary team with expertise in statistics, bioinformatics, modeling and computer science to provide broad support capabilities in this Research Support Core. In the first three years of this SRP, Core C has provided invaluable support in all aspects of the research. From experimental design to multivariate integration, from bioinformatics to regulatory networks, and from data management to customized software solutions, our Core has facilitated scientific advancement in the research projects and enabled data integration across multiple research projects. In the next five years, we propose to continue our support of the program, providing sophisticated data analyses and expand our efforts into more predictive, computational modeling through three primary specific aims; 1) biostatistics support to facilitate linkage of exposure (source) to phenotype (outcome) for chemical mixtures, 2) predictive modeling and informatics for mechanistic evaluation of mixtures, and 3) customized software solutions for data processing and integrations. Core C ensures statistically robust experimental design, standardized data pipelines, data integration and results interpretation across all research projects and cores to ensure robust measurement of exposure, dose, response and phenotype and achieve source to outcome linkage for science-based risk assessment. Multidisciplinary training of toxicology students and postdoctoral fellows in statistics and bioinformatics also assures that the next generation of researchers and professionals tasked with protecting human health and the environment from the risks of hazardous substances will possess the skills to analyze and interpret their own data.

Public Health Relevance

Assessing the health effects of PAHs is a major challenge because environmental exposures to these chemicals are usually complex mixtures of PAHs and often other toxicants. Integration of exposure data with biological activity and pharmacokinetics is essential to evaluate the effects presented by these chemical mixtures on human health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES016465-07
Application #
8837636
Study Section
Special Emphasis Panel (ZES1-LWJ-D)
Project Start
Project End
Budget Start
2015-04-01
Budget End
2016-03-31
Support Year
7
Fiscal Year
2015
Total Cost
$463,645
Indirect Cost
Name
Oregon State University
Department
Type
DUNS #
053599908
City
Corvallis
State
OR
Country
United States
Zip Code
97331
Balik-Meisner, Michele; Truong, Lisa; Scholl, Elizabeth H et al. (2018) Elucidating Gene-by-Environment Interactions Associated with Differential Susceptibility to Chemical Exposure. Environ Health Perspect 126:067010
Geier, Mitra C; James Minick, D; Truong, Lisa et al. (2018) Systematic developmental neurotoxicity assessment of a representative PAH Superfund mixture using zebrafish. Toxicol Appl Pharmacol 354:115-125
Tan, Yu-Mei; Leonard, Jeremy A; Edwards, Stephen et al. (2018) Aggregate Exposure Pathways in Support of Risk Assessment. Curr Opin Toxicol 9:8-13
Titaley, Ivan A; Ogba, O Maduka; Chibwe, Leah et al. (2018) Automating data analysis for two-dimensional gas chromatography/time-of-flight mass spectrometry non-targeted analysis of comparative samples. J Chromatogr A 1541:57-62
Geier, Mitra C; Chlebowski, Anna C; Truong, Lisa et al. (2018) Comparative developmental toxicity of a comprehensive suite of polycyclic aromatic hydrocarbons. Arch Toxicol 92:571-586
Bugel, Sean M; Tanguay, Robert L (2018) Multidimensional chemobehavior analysis of flavonoids and neuroactive compounds in zebrafish. Toxicol Appl Pharmacol 344:23-34
Garcia, Gloria R; Bugel, Sean M; Truong, Lisa et al. (2018) AHR2 required for normal behavioral responses and proper development of the skeletal and reproductive systems in zebrafish. PLoS One 13:e0193484
Roper, Courtney; Simonich, Staci L Massey; Tanguay, Robert L (2018) Development of a high-throughput in vivo screening platform for particulate matter exposures. Environ Pollut 235:993-1005
Haggard, Derik E; Noyes, Pamela D; Waters, Katrina M et al. (2018) Transcriptomic and phenotypic profiling in developing zebrafish exposed to thyroid hormone receptor agonists. Reprod Toxicol 77:80-93
Hummel, Jessica M; Madeen, Erin P; Siddens, Lisbeth K et al. (2018) Pharmacokinetics of [14C]-Benzo[a]pyrene (BaP) in humans: Impact of Co-Administration of smoked salmon and BaP dietary restriction. Food Chem Toxicol 115:136-147

Showing the most recent 10 out of 174 publications