9600796 Miller The E. coli genome analysis efforts are likely to achieve a complete sequence determination of the well studied organism by the end of 1996. Over 2800 genes and ORFs have been sequenced; over 70% of the chromosomal DNA, and their gene products, where identified, are in the Swiss Protein database. The extensive genetic, physiological and biochemical knowledge of E. coli make this the best defined of all organisms. There is much excitement surrounding the opportunity now to integrate these bodies of information as we approach total sequence of E. coli DNA and all gene products. Moreover, there is the added excitement of being able to compare the E. coli sequence with that of as many as 10 other small genomes. To carry out the integration, scientists working on E. coli in different areas will interact. The sequencers, cloners, geneticists, cell physiologists, biochemists, database builders and computer scientists all come from different perspectives that are now fusing. The meeting will facilitate the necessary interactions by bringing together leading researchers in the analysis of genomes at the genetic and sequence level, and will facilitate the coordination of the structural and functional analysis of this organism's genome. Participants in the complete sequencing of H. influenzae, mycoplasma, and 7 different archaea will also present their findings, affording the unprecedented opportunity to compare results from so many completed genomes. This meeting is designed to have a mix of invited and participant-initiated presentations, and will also have hands-on workshops during which investigators from different disciplines will be able to become familiar with available databases and new tools facilitating analysis and coordination of information. Participants will not only hear the latest information in the talks, but also will have available hands-on instruction in new computer-based abilities to seek out and capture, analyze, correlate and integrate complex new information. The fields are moving very fast both in acquisition of new knowledge of the contents of genomes and their significance to cellular processes and also in management and analysis of the information, connecting bodies of knowledge on sequences, genetic organization and regulation. No other meeting synthesizes the biology of E. coli, sequence information and database analysis, as well as the comparison with other completed genome sequences. ***

Agency
National Science Foundation (NSF)
Institute
Division of Molecular and Cellular Biosciences (MCB)
Type
Standard Grant (Standard)
Application #
9600796
Program Officer
Philip Harriman
Project Start
Project End
Budget Start
1996-09-01
Budget End
1997-08-31
Support Year
Fiscal Year
1996
Total Cost
$5,500
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
City
Los Angeles
State
CA
Country
United States
Zip Code
90095