Evidence map›Paper›PMID 17683565›Full record

ArticleBMC bioinformatics2007

Bayesian hierarchical model for transcriptional module discovery by jointly modeling gene expression and ChIP-chip data.

Xiangdong Liu, Walter J Jessen, Siva Sivaganesan, Bruce J Aronow, Mario Medvedovic

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Computational methodology for ChIP-seq analysis.Quantitative biology (Beijing, China) · 2013
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. CLEAN: CLustering Enrichment ANalysis.BMC bioinformatics · 2009
    Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Xiangdong LiuDepartment of Environmental Health, University of Cincinnati, 3223 Eden Ave, ML 56, Cincinnati, Ohio 45267, USA. xiangdong.liu@cchmc.org
Walter J Jessen
Siva Sivaganesan
Bruce J Aronow
Mario Medvedovic

Funding

Bayesian Mixture Modeling of Functional Genomics DataR01HG003749 · NHGRI · UNIVERSITY OF CINCINNATI · PI MEDVEDOVIC, MARIO · 2006 to 2009
$1.4M
Joint Modeling of Genomic and Functional Genomic DataR03LM008248 · NLM · UNIVERSITY OF CINCINNATI · PI MEDVEDOVIC, MARIO · 2004 to 2005
$154k
NHGRI NIH HHS 1R01HG003749NHGRI NIH HHS R01 HG003749NLM NIH HHS 1R03LM008248NLM NIH HHS R03 LM008248
6 · The paper itself

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.

Indexed as

AlgorithmsModels, GeneticArtificial IntelligenceBayes TheoremChromatin ImmunoprecipitationChromosome MappingDatabases, GeneticGene Expression ProfilingInformation Storage and RetrievalOligonucleotide Array Sequence AnalysisSequence Analysis, DNATranscription FactorsTranscription Factors

Identifiers

PMID17683565
PMCPMC1994961

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.