Lyle D. Burgoon
Visiting Research Associate

Contact information
248 National Food Safety & Toxicology Center
Phone: 517-432-3100 ext. 189
burgoonl@msu.edu

Education

Ph.D., Michigan State University, Pharmacology and Toxicology with Environmental Toxicology, 2005

A.B. Augustana College, Rock Island, IL, Pre-Medicine and Biology, Cum Laude, 1999


Research Interests
Systems toxicology in drug and chemical regulatory and quantitative safety assessment; analysis, experimental design, and management of massive datasets; computational and quantitative toxicology and pathology to identify novel agglomerative biomarkers of exposure and toxicity; science policy with regards to dual-use of toxicological data.

Research Projects

1) Toxicogenomic data investigation and visualization. These projects include development of novel methods of data analysis, experimental design, data management, mining, and visualization. These include the use and development of clustering technologies and visualizing these data in novel ways. This also includes data fusion (fusion of data from disparate data domains with regards to the same exposure) to identify novel agglomerative biomarkers of toxicity and exposure.

2) Metabolomics. Metabolomics serves as a new thrust area for the laboratory. I am taking the lead in developing NMR and metabolomic skills and protocols to support laboratory interests in this area. Future work will include the development of rigourous statistical and machine learning methods for the near automation of data analysis, and speeding the time to knowledge from this technology. Data derived from this activity will directly influence our data fusion and other mining and visualization activities.

3) Functional regulatory element prediction and identification. This project leverages the dbZach database to identify regulatory elements that may predict or further explain a gene's response to a chemical exposure. This project further drives the mechanistic research within the laboratory, and expands the services available to the researchers within the laboratory.

4) Computational and Quantitative Pathology. This is a thrust area within the lab that seeks to leverage the Histopathology Management functions within the dbZach System. The goals are to develop a histology image bank of normal and diseased tissues for the automated discovery of lesions. Future work in this area will also include lesion discovery.

5) Development of the dbZach System. The dbZach System is a data management, analysis, mining, and visualization system for toxicology and allied data. I am the primary architect of the system, and the lead developer. Future technologies that will be supported include metabonomics and proteomics.

6) Development and maintenance of our toxicogenomic information technology infrastructure. As the lead bioinformatician for the Zacharewski Lab Bioinformatics Group I also take the lead on procuring and maintaining our Bio-IT infrastructure. Our greatest achievement was the procurement of two IBM x255 eServers; one for database management, the second for analysis.

In addition to these projects, I am also involved in the microarray community at-large. I am a member of, and a consultant, to the International Life Sciences Institute (ILSI) Heath and Environmental Sciences Institute (HESI) Committee on Application of Genomics to Mechanism Based Risk Assessment. I'm also a member of the Toxicogenomics Working Group of the Microarray Gene Expression Data Society. In the past I have lectured on microarray database development, large-scale biological data management, and reproductive and developmental toxicology.