Evidence map›Paper›PMID 22595208›Full record

ArticleBioinformatics (Oxford, England)2012

Robust identification of transcriptional regulatory networks using a Gibbs sampler on outlier sum statistic.

Jinghua Gu, Jianhua Xuan, Rebecca B Riggins, Li Chen, Yue Wang, Robert Clarke

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Antiestrogen Resistance and the Application of Systems Biology.Drug discovery today. Disease mechanisms · 2012
    Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Jinghua GuBradley Department of Electrical and Computer Engineering, Virginia Tech, Arlington, VA 22203, USA.
Jianhua Xuan
Rebecca B Riggins
Li Chen
Yue Wang
Robert Clarke
Georgetown University · USVirginia Tech · US

Funding

Novel Targets in Endocrine ResponsivenessU54CA149147 · NCI · GEORGETOWN UNIVERSITY · PI CLARKE, ROBERT R. · 2010 to 2014
$6.9M
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
Uncovering Estrogen Receptor-Signaling Networks to Overcome Endocrine ResistanceR01CA149653 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI XUAN, JASON JIANHUA · 2011 to 2015
$1.5M
Comprehensive Analysis of Microarray Gene ExpressionR33CA109872 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WANG, YUE · 2005 to 2007
$1.4M
Network-based Prediction of Antiestrogen Resistance in Breast CancerR21CA139246 · NCI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI XUAN, JASON JIANHUA · 2009 to 2010
$381k
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 CA139246NCI NIH HHS CA149147NCI NIH HHS CA149653NINDS NIH HHS NS29525-13ANINDS NIH HHS NS29525-18APHS HHS HHSN261200800001E
6 · The paper itself

Abstract

motivationIdentification of transcriptional regulatory networks (TRNs) is of significant importance in computational biology for cancer research, providing a critical building block to unravel disease pathways. However, existing methods for TRN identification suffer from the inclusion of excessive 'noise' in microarray data and false-positives in binding data, especially when applied to human tumor-derived cell line studies. More robust methods that can counteract the imperfection of data sources are therefore needed for reliable identification of TRNs in this context.

resultsIn this article, we propose to establish a link between the quality of one target gene to represent its regulator and the uncertainty of its expression to represent other target genes. Specifically, an outlier sum statistic was used to measure the aggregated evidence for regulation events between target genes and their corresponding transcription factors. A Gibbs sampling method was then developed to estimate the marginal distribution of the outlier sum statistic, hence, to uncover underlying regulatory relationships. To evaluate the effectiveness of our proposed method, we compared its performance with that of an existing sampling-based method using both simulation data and yeast cell cycle data. The experimental results show that our method consistently outperforms the competing method in different settings of signal-to-noise ratio and network topology, indicating its robustness for biological applications. Finally, we applied our method to breast cancer cell line data and demonstrated its ability to extract biologically meaningful regulatory modules related to estrogen signaling and action in breast cancer. AVAILABILITY AND IMPLEMENTATION: The Gibbs sampler MATLAB package is freely available at http://www.cbil.ece.vt.edu/software.htm. CONTACT: xuan@vt.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Gene Regulatory NetworksSoftwareBreast NeoplasmsCell CycleCell Line, TumorComputational BiologyComputer SimulationFemaleGene Expression Regulation, NeoplasticHumansSignal-To-Noise RatioSignal TransductionTranscription FactorsTranscription Factors

Identifiers

PMID22595208
PMCPMC3400952
OpenAlexW2134644261

What OpenQuestion holds

Textmetadata
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.