ArticleBMC bioinformatics2007
Bayesian hierarchical model for transcriptional module discovery by jointly modeling gene expression and ChIP-chip data.
Article in BMC bioinformatics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Integrated genomic analysis of biological gene sets with applications in lung cancer prognosis.BMC bioinformatics · 2017Article
- Computational methodology for ChIP-seq analysis.Quantitative biology (Beijing, China) · 2013Article
- Bayesian correlated clustering to integrate multiple datasets.Bioinformatics (Oxford, England) · 2012Article
- Systematically characterizing and prioritizing chemosensitivity related gene based on Gene Ontology and protein interaction network.BMC medical genomics · 2012Article
- Learning transcriptional networks from the integration of ChIP-chip and expression data in a non-parametric model.Bioinformatics (Oxford, England) · 2010Article
- Discovering transcriptional modules by Bayesian data integration.Bioinformatics (Oxford, England) · 2010Article
- A semi-parametric Bayesian model for unsupervised differential co-expression analysis.BMC bioinformatics · 2010Article
- Reconstructing transcriptional regulatory networks through genomics data.Statistical methods in medical research · 2009Article
- CLEAN: CLustering Enrichment ANalysis.BMC bioinformatics · 2009Article
- Transcriptional programs: modelling higher order structure in transcriptional control.BMC bioinformatics · 2009Article
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5 authors.
Funding
Abstract
backgroundTranscriptional modules (TM) consist of groups of co-regulated genes and transcription factors (TF) regulating their expression. Two high-throughput (HT) experimental technologies, gene expression microarrays and Chromatin Immuno-Precipitation on Chip (ChIP-chip), are capable of producing data informative about expression regulatory mechanism on a genome scale. The optimal approach to joint modeling of data generated by these two complementary biological assays, with the goal of identifying and characterizing TMs, is an important open problem in computational biomedicine.
resultsWe developed and validated a novel probabilistic model and related computational procedure for identifying TMs by jointly modeling gene expression and ChIP-chip binding data. We demonstrate an improved functional coherence of the TMs produced by the new method when compared to either analyzing expression or ChIP-chip data separately or to alternative approaches for joint analysis. We also demonstrate the ability of the new algorithm to identify novel regulatory relationships not revealed by ChIP-chip data alone. The new computational procedure can be used in more or less the same way as one would use simple hierarchical clustering without performing any special transformation of data prior to the analysis. The R and C-source code for implementing our algorithm is incorporated within the R package gimmR which is freely available at http://eh3.uc.edu/gimm.
conclusionOur results indicate that, whenever available, ChIP-chip and expression data should be analyzed within the unified probabilistic modeling framework, which will likely result in improved clusters of co-regulated genes and improved ability to detect meaningful regulatory relationships. Given the good statistical properties and the ease of use, the new computational procedure offers a worthy new tool for reconstructing transcriptional regulatory networks.
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