PROSPECT improves cis-acting regulatory element prediction by integrating expression profile data with consensus pattern searches
Author(s) -
Wataru Fujibuchi,
John S. J. Anderson,
David Landsman
Publication year - 2001
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/29.19.3988
Subject(s) - biology , false positive paradox , computational biology , consensus sequence , regulatory sequence , gene , ranking (information retrieval) , expression (computer science) , similarity (geometry) , genetics , dna microarray , phenotype , probabilistic logic , gene expression , metric (unit) , data mining , artificial intelligence , computer science , base sequence , operations management , economics , image (mathematics) , programming language
Consensus pattern and matrix-based searches designed to predict cis-acting transcriptional regulatory sequences have historically been subject to large numbers of false positives. We sought to decrease false positives by incorporating expression profile data into a consensus pattern-based search method. We have systematically analyzed the expression phenotypes of over 6000 yeast genes, across 121 expression profile experiments, and correlated them with the distribution of 14 known regulatory elements over sequences upstream of the genes. Our method is based on a metric we term probabilistic element assessment (PEA), which is a ranking of potential sites based on sequence similarity in the upstream regions of genes with similar expression phenotypes. For eight of the 14 known elements that we examined, our method had a much higher selectivity than a naïve consensus pattern search. Based on our analysis, we have developed a web-based tool called PROSPECT, which allows consensus pattern-based searching of gene clusters obtained from microarray data.
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