Evidence map›Paper›PMID 18315853›Full record

ArticleBMC bioinformatics2008

Motif-directed network component analysis for regulatory network inference.

Chen Wang, Jianhua Xuan, Li Chen, Po Zhao, Yue Wang, Robert Clarke, Eric Hoffman

Abstract read
In one paragraph

Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

7 authors.

Chen WangDepartment of Electrical and Computer Engineering, Virginia Polytechnic Institute and State University, Arlington, VA, USA. topsoil@vt.edu
Jianhua Xuan
Li Chen
Po Zhao
Yue Wang
Robert Clarke
Eric Hoffman

Funding

Improved Diagnostic of the Muscular DystrophiesR01NS029525 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HOFFMAN, ERIC P. · 1991 to 2015
$6.5M
Molecular Analysis of Human Breast CancerR01CA096483 · NCI · GEORGETOWN UNIVERSITY · PI CLARKE, ROBERT R. · 2003 to 2007
$2.5M
Compute Decomposition/Composite Molecular SignaturesR33EB000830 · NIBIB · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2005 to 2007
$1.6M
Comprehensive Analysis of Microarray Gene ExpressionR33CA109872 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2005 to 2007
$1.4M
Compute Decomposition/Composite Molecular SignaturesR21EB000830 · NIBIB · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2003 to 2004
$266k
Comprehensive Analysis of Microarray Gene ExpressionR21CA109872 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2004 to 2004
$149k
NCI NIH HHS CA096483NCI NIH HHS CA109872NCI NIH HHS R01 CA096483NCI NIH HHS R21 CA109872NCI NIH HHS R33 CA109872NIBIB NIH HHS EB000830NIBIB NIH HHS R21 EB000830NIBIB NIH HHS R33 EB000830NINDS NIH HHS NS29525-13ANINDS NIH HHS R01 NS029525
6 · The paper itself

Abstract

backgroundNetwork Component Analysis (NCA) has shown its effectiveness in discovering regulators and inferring transcription factor activities (TFAs) when both microarray data and ChIP-on-chip data are available. However, a NCA scheme is not applicable to many biological studies due to limited topology information available, such as lack of ChIP-on-chip data. We propose a new approach, motif-directed NCA (mNCA), to integrate motif information and gene expression data to infer regulatory networks.

resultsWe develop motif-directed NCA (mNCA) to incorporate motif information into NCA for regulatory network inference. While motif information is readily available from knowledge databases, it is a "noisy" source of network topology information consisting of many false positives. To overcome this problem, we develop a stability analysis procedure embedded in mNCA to resolve the inconsistency between motif information and gene expression data, and to enable the identification of stable TFAs. The mNCA approach has been applied to a time course microarray data set of muscle regeneration. The experimental results show that the inferred TFAs are not only numerically stable but also biologically relevant to muscle differentiation process. In particular, several inferred TFAs like those of MyoD, myogenin and YY1 are well supported by biological experiments.

conclusionA novel computational approach, mNCA, has been developed to integrate motif information and gene expression data for regulatory network reconstruction. Specifically, motif analysis is used to obtain initial network topology, and stability analysis is developed and applied with mNCA to extract stable TFAs. Experimental results on muscle regeneration microarray data have demonstrated that mNCA is a practical and reliable computational method for regulatory network inference and pathway discovery.

Indexed as

Models, GeneticBase SequenceComputer SimulationGene Expression ProfilingGene Expression RegulationMolecular Sequence DataOligonucleotide Array Sequence AnalysisSequence Analysis, DNASignal TransductionTranscription FactorsTranscription Factors

Identifiers

PMID18315853
PMCPMC2259422

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.