The wealth of information that is now available from the sequencing of the human genome holds great promise for understanding the genetically-based mechanisms that contribute to disease. Extracting maximum benefit from genome sequence requires the most complete and accurate annotation possible. The general goal of my research is to develop new probability models for gene prediction based on the maximum entropy principle. A benefit of this work will be improved software tools for annotators to use for automated gene-structure prediction or computer support for manual annotation. A specific goal is to apply the improved tools to gene prediction in the pathogenic fungus cryptococcus neoformans responsible for opportunistic infections in immuno-compromised patients. Some of the predicted genes will be cloned by a collaborator, Dr. Tamara Doering, providing experimental feedback on the efficacy of the predictions and contributing to our understanding of a disease process and, hopefully, to the development of drugs to combat cryptococcus infections.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
National Research Service Awards for Senior Fellows (F33)
Project #
1F33HG002635-01
Application #
6551937
Study Section
Genome Study Section (GNM)
Program Officer
Graham, Bettie
Project Start
2002-12-02
Project End
2004-12-01
Budget Start
2002-12-02
Budget End
2003-12-01
Support Year
1
Fiscal Year
2003
Total Cost
$56,308
Indirect Cost
Name
Washington University
Department
Biostatistics & Other Math Sci
Type
Schools of Engineering
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Brown, Randall H; Gross, Samuel S; Brent, Michael R (2005) Begin at the beginning: predicting genes with 5' UTRs. Genome Res 15:742-7