Home LiteratureArticle Details
PMID: 15308537 Published · ppublish English Comparative Study Evaluation Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Validation Study

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

Bioinformatics (Oxford, England) ·Vol. 21 ·No. 1 ·2005-01-01 ·Pages 71-9

Zou M, Conzen SD

Abstract

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. 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.

MeSH Terms
Algorithms Bayes Theorem Cell Cycle Proteins/metabolism Computer Simulation Gene Expression Profiling/methods Gene Expression Regulation/physiology Models, Biological Models, Statistical Oligonucleotide Array Sequence Analysis/methods Saccharomyces cerevisiae/metabolism Saccharomyces cerevisiae Proteins/metabolism Signal Transduction/physiology Time Factors Transcription Factors/metabolism
Chemicals
Cell Cycle Proteins Saccharomyces cerevisiae Proteins Transcription Factors
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zou Min
Department of Medicine, 5841 South Maryland Avenue, University of Chicago, Chicago, IL 60637, USA.
Conzen Suzanne D
Article Info
Journal
Bioinformatics (Oxford, England)
Abbr.
Bioinformatics
ISSN
1367-4803
Published
2005-01-01
Epub
2004-00-12
Pages
71-9
Language
English
Region
England
NLM ID
9808944
Subset
IM
Grants
NCI NIH HHS · CA89208 · United States
NCI NIH HHS · CA90459 · United States
NIEHS NIH HHS · ES0123282 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com