Evidence map›Paper›PMID 27294826›Full record

ArticleBMC bioinformatics2016

A comparative evaluation of data-merging and meta-analysis methods for reconstructing gene-gene interactions.

Vincenzo Lagani, Argyro D Karozou, David Gomez-Cabrero, Gilad Silberberg, Ioannis Tsamardinos

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2016. 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

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  12. Evidence for shared molecular pathways of dysregulated decidualization in preeclampsia and endometrial disorders revealed by microarray data integration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Vincenzo LaganiInstitute of Computer Science, Foundation for Research and Technology - Hellas, Heraklion, Greece.
Argyro D KarozouInstitute of Computer Science, Foundation for Research and Technology - Hellas, Heraklion, Greece.
David Gomez-CabreroUnit of Computational Medicine, Department of Medicine, Karolinska Institutet, 171 77, Stockholm, Sweden.
Gilad SilberbergUnit of Computational Medicine, Department of Medicine, Karolinska Institutet, 171 77, Stockholm, Sweden.
Ioannis TsamardinosInstitute of Computer Science, Foundation for Research and Technology - Hellas, Heraklion, Greece. tsamard@csd.uoc.gr.
Foundation for Research and Technology Hellas · GRKarolinska Institutet · SEScience for Life Laboratory · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe address the problem of integratively analyzing multiple gene expression, microarray datasets in order to reconstruct gene-gene interaction networks. Integrating multiple datasets is generally believed to provide increased statistical power and to lead to a better characterization of the system under study. However, the presence of systematic variation across different studies makes network reverse-engineering tasks particularly challenging. We contrast two approaches that have been frequently used in the literature for addressing systematic biases: meta-analysis methods, which first calculate opportune statistics on single datasets and successively summarize them, and data-merging methods, which directly analyze the pooled data after removing eventual biases. This comparative evaluation is performed on both synthetic and real data, the latter consisting of two manually curated microarray compendia comprising several E. coli and Yeast studies, respectively. Furthermore, the reconstruction of the regulatory network of the transcription factor Ikaros in human Peripheral Blood Mononuclear Cells (PBMCs) is presented as a case-study.

resultsThe meta-analysis and data-merging methods included in our experimentations provided comparable performances on both synthetic and real data. Furthermore, both approaches outperformed (a) the naïve solution of merging data together ignoring possible biases, and (b) the results that are expected when only one dataset out of the available ones is analyzed in isolation. Using correlation statistics proved to be more effective than using p-values for correctly ranking candidate interactions. The results from the PBMC case-study indicate that the findings of the present study generalize to different types of network reconstruction algorithms.

conclusionsIgnoring the systematic variations that differentiate heterogeneous studies can produce results that are statistically indistinguishable from random guessing. Meta-analysis and data merging methods have proved equally effective in addressing this issue, and thus researchers may safely select the approach that best suit their specific application.

Indexed as

AlgorithmsArea Under CurveEscherichia coliGene Regulatory NetworksHumansLeukocytes, MononuclearMeta-Analysis as TopicROC CurveSaccharomyces cerevisiaeBatch-effect RemovalEscherichia coliGene-network ReconstructionIkaros Transcription FactorIntegrative AnalysisMeta-AnalysisPeripheral Blood Mononuclear CellsSurrogate Variable AnalysisYeast

Identifiers

PMID27294826
PMCPMC4905611
OpenAlexW2413346047

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.