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Nucleic Acids Research 2004 32(12):3581-3589; doi:10.1093/nar/gkh681
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Published online 7 July 2004

Nucleic Acids Research, Vol. 32 No. 12 © Oxford University Press 2004; all rights reserved

New strategy for the representation and the integration of biomolecular knowledge at a cellular scale

Roland Barriot1,2, Jérôme Poix3, Alexis Groppi1, Aurélien Barré1, Nicolas Goffard1, David Sherman1,2, Isabelle Dutour1,2 and Antoine de Daruvar1,*

1 Centre de Bioinformatique de Bordeaux, Université V. Segalen Bordeaux 2, 146 rue Léo Saignat, 33076 Bordeaux, France, 2 LaBRI, Laboratoire Bordelais de Recherche en Informatique, UMR CNRS 5800, 351 cours de la Libération, 33405 Talence Cedex, France and 3 Laboratoire Statistique Mathématique et ses Applications, EA 2961, Université V. Segalen Bordeaux 2, 146 rue Léo Saignat, 33076 Bordeaux, France

* To whom correspondence should be addressed. Tel: +33 5 57 57 12 47; Fax: +33 5 57 57 12 47; Email: antoine.daruvar{at}pmtg.u-bordeaux2.fr

Received March 8, 2004; Revised and Accepted June 4, 2004

The combination of sequencing and post-sequencing experimental approaches produces huge collections of data that are highly heterogeneous both in structure and in semantics. We propose a new strategy for the integration of such data. This strategy uses structured sets of sequences as a unified representation of biological information and defines a probabilistic measure of similarity between the sets. Sets can be composed of sequences that are known to have a biological relationship (e.g. proteins involved in a complex or a pathway) or that share similar values for a particular attribute (e.g. expression profile). We have developed a software, BlastSets, which implements this strategy. It exploits a database where the sets derived from diverse biological information can be deposited using a standard XML format. For a given query set, BlastSets returns target sets found in the database whose similarity to the query is statistically significant. The tool allowed us to automatically identify verified relationships between correlated expression profiles and biological pathways using publicly available data for Saccharomyces cerevisiae. It was also used to retrieve the members of a complex (ribosome) based on the mining of expression profiles. These first results validate the relevance of the strategy and demonstrate the promising potential of BlastSets.


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