Evidence map›Paper›PMID 18980677›Full record

ArticleBMC bioinformatics2008

Learning transcriptional regulatory networks from high throughput gene expression data using continuous three-way mutual information.

Weijun Luo, Kurt D Hankenson, Peter J Woolf

Open access · goldAbstract 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 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

33 citing papers in PubMed, 80 citations in OpenAlex.

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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

3 authors at 2 institutions in 1 country.

Weijun LuoDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA. luo@cshl.edu
Kurt D Hankenson
Peter J Woolf
University of Michigan–Ann Arbor · USUniversity of Pennsylvania · US

Funding

Nation Center- Integrative Biomedical Informatics(RMI)U54DA021519 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATHEY, BRIAN DAVID · 2005 to 2010
$21.3M
Endosteal Adipose in Age-Associated OsteopeniaR01AR054714 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI HANKENSON, KURT DAVID · 2006 to 2010
$1.9M
BMP6 Induction of Human Mesenchymal Stem Cell Osteoblast DifferentiationR01DE017471 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI HANKENSON, KURT DAVID · 2006 to 2010
$1.9M
Matricellular Proteins and Mesenchymal Stem CellsR01AR049682 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI HANKENSON, KURT DAVID · 2002 to 2006
$1.2M
NIAMS NIH HHS R01 AR049682NIAMS NIH HHS R01 AR054714NIDA NIH HHS U54 DA021519NIDA NIH HHS U54-DA-021519NIDCR NIH HHS R01 DE017471
6 · The paper itself

Abstract

backgroundProbability based statistical learning methods such as mutual information and Bayesian networks have emerged as a major category of tools for reverse engineering mechanistic relationships from quantitative biological data. In this work we introduce a new statistical learning strategy, MI3 that addresses three common issues in previous methods simultaneously: (1) handling of continuous variables, (2) detection of more complex three-way relationships and (3) better differentiation of causal versus confounding relationships. With these improvements, we provide a more realistic representation of the underlying biological system.

resultsWe test the MI3 algorithm using both synthetic and experimental data. In the synthetic data experiment, MI3 achieved an absolute sensitivity/precision of 0.77/0.83 and a relative sensitivity/precision both of 0.99. In addition, MI3 significantly outperformed the control methods, including Bayesian networks, classical two-way mutual information and a discrete version of MI3. We then used MI3 and control methods to infer a regulatory network centered at the MYC transcription factor from a published microarray dataset. Models selected by MI3 were numerically and biologically distinct from those selected by control methods. Unlike control methods, MI3 effectively differentiated true causal models from confounding models. MI3 recovered major MYC cofactors, and revealed major mechanisms involved in MYC dependent transcriptional regulation, which are strongly supported by literature. The MI3 network showed that limited sets of regulatory mechanisms are employed repeatedly to control the expression of large number of genes.

conclusionOverall, our work demonstrates that MI3 outperforms the frequently used control methods, and provides a powerful method for inferring mechanistic relationships underlying biological and other complex systems. The MI3 method is implemented in R in the "mi3" package, available under the GNU GPL from http://sysbio.engin.umich.edu/~luow/downloads.php and from the R package archive CRAN.

Indexed as

AlgorithmsArtificial IntelligenceGene ExpressionGene Regulatory NetworksSystems Biology

Identifiers

PMID18980677
PMCPMC2613931
OpenAlexW2069986908

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.