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Treffer: A new dynamic Bayesian network (DBN) approach for identifying gene regulatory networks from time course microarray data.

Title:
A new dynamic Bayesian network (DBN) approach for identifying gene regulatory networks from time course microarray data.
Authors:
Zou M; Department of Medicine, 5841 South Maryland Avenue, University of Chicago, Chicago, IL 60637, USA., Conzen SD
Source:
Bioinformatics (Oxford, England) [Bioinformatics] 2005 Jan 01; Vol. 21 (1), pp. 71-9. Date of Electronic Publication: 2004 Aug 12.
Publication Type:
Comparative Study; Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Validation Study
Language:
English
Journal Info:
Publisher: Oxford University Press Country of Publication: England NLM ID: 9808944 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1367-4803 (Print) Linking ISSN: 13674803 NLM ISO Abbreviation: Bioinformatics Subsets: MEDLINE
Imprint Name(s):
Original Publication: Oxford : Oxford University Press, c1998-
Grant Information:
CA89208 United States CA NCI NIH HHS; CA90459 United States CA NCI NIH HHS; ES0123282 United States ES NIEHS NIH HHS
Substance Nomenclature:
0 (Cell Cycle Proteins)
0 (Saccharomyces cerevisiae Proteins)
0 (Transcription Factors)
Entry Date(s):
Date Created: 20040817 Date Completed: 20050308 Latest Revision: 20220321
Update Code:
20250114
DOI:
10.1093/bioinformatics/bth463
PMID:
15308537
Database:
MEDLINE

Weitere Informationen

Motivation: Signaling pathways are dynamic events that take place over a given period of time. In order to identify these pathways, expression data over time are required. Dynamic Bayesian network (DBN) is an important approach for predicting the gene regulatory networks from time course expression data. However, two fundamental problems greatly reduce the effectiveness of current DBN methods. The first problem is the relatively low accuracy of prediction, and the second is the excessive computational time.
Results: In this paper, we present a DBN-based approach with increased accuracy and reduced computational time compared with existing DBN methods. Unlike previous methods, our approach limits potential regulators to those genes with either earlier or simultaneous expression changes (up- or down-regulation) in relation to their target genes. This allows us to limit the number of potential regulators and consequently reduce the search space. Furthermore, we use the time difference between the initial change in the expression of a given regulator gene and its potential target gene to estimate the transcriptional time lag between these two genes. This method of time lag estimation increases the accuracy of predicting gene regulatory networks. Our approach is evaluated using time-series expression data measured during the yeast cell cycle. The results demonstrate that this approach can predict regulatory networks with significantly improved accuracy and reduced computational time compared with existing DBN approaches.