DocumentCode :
2528297
Title :
cis-Regulatory element prediction in mammalian genomes
Author :
Siddiqui, Asim ; Robertson, Gordon ; Bilenky, Misha ; Astakhova, Tamara ; Griffith, Obi L. ; Hassel, Maik ; Lin, Keven ; Montgomery, Stephen ; Oveisi, Mehrdad ; Pleasance, Erin ; Robertson, Neil ; Sleumer, Monica C. ; Teague, Kevin ; Varhol, Richard ; Zha
Author_Institution :
Canada´´s Michael Smith Genome Sci. Centre, British Columbia Cancer Res. Centre, Vancouver, BC, Canada
fYear :
2005
fDate :
8-11 Aug. 2005
Firstpage :
203
Lastpage :
204
Abstract :
The identification of cis-regulatory elements and modules is an important step in understanding the regulation of genes. We have developed a pipeline capable of running multiple motif prediction methods on a whole genome scale. Using gene expression datasets to identify co-expressed genes and the Ensemhl Compara database orthologues, we assemble input sequence sets comprised of the upstream regions of a target gene, its orthologues and co-expressed genes on the premise that such genes will share promoters by evolution (orthologues) or share regulatory control mechanisms (co-expressed genes). Co-expressed genes are identified by an approach that combines Pearson distances from multiple gene expression datasets derived from multiple experimental approaches and calibrated against the GO database. Our pipeline runs a number of established motif detection algorithms with a range of parameter settings on the input dataset. We integrate the diverse result sets by scoring motifs with a method-independent function. For each target gene, we assign p-values to the motif score by running the discovery pipeline on multiple sets of input sequence containing the target gene, non-coexpressed genes and "Jake" orthologues generated by neutral numerical evolution. We have predicted 30,636 motif binding sites in human for 4,182 genes and an initial set of 472 motif binding sites in mouse for 92 genes with p<0.001. The positive predictive value against a library of biologically confirmed regulatory sites approaches 0.4 at the highest p-value threshold. Predicted regulatory elements and other resources from the project are available at www.cisred.org.
Keywords :
biology computing; genetics; prediction theory; Ensemhl Compara database orthologue; Pearson distance; biological confirmed regulatory site; cis-regulatory element; cis-regulatory element prediction; coexpressed genes; gene expression dataset; gene regulation; genome scale; highest p-value threshold; input sequence set; mammalian genomes; motif binding sites; motif detection algorithm; multiple gene expression datasets; multiple motif prediction methods; neutral numerical evolution; parameter setting; positive predictive value; share regulatory control mechanism; Assembly; Bioinformatics; Databases; Detection algorithms; Evolution (biology); Gene expression; Genomics; Humans; Pipelines; Prediction methods;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Computational Systems Bioinformatics Conference, 2005. Workshops and Poster Abstracts. IEEE
Print_ISBN :
0-7695-2442-7
Type :
conf
DOI :
10.1109/CSBW.2005.35
Filename :
1540599
Link To Document :
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