Evidence map›Paper›PMID 24658540›Full record

ArticlePloS one2014

Selection of higher order regression models in the analysis of multi-factorial transcription data.

Olivia Prazeres da Costa, Arthur Hoffman, Johannes W Rey, Ulrich Mansmann, Thorsten Buch, Achim Tresch

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-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

0 citing papers in PubMed, 7 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 5 institutions in 1 country.

Olivia Prazeres da CostaInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
Arthur HoffmanSt. Mary's hospital, Department of Medicine, Frankfurt, Germany; Medical Department, Johannes Gutenberg University, Mainz, Germany.
Johannes W ReyMedical Department, Johannes Gutenberg University, Mainz, Germany.
Ulrich MansmannInstitute for Medical Informatics, Biometry and Epidemiology (IBE), Ludwig-Maximilians-Universität München, Munich, Germany.
Thorsten BuchInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.
Achim TreschDepartment of Plant Breeding and Genetics, Max Planck Institute for Plant Breeding Research, Cologne, Germany; Institute for Genetics, University of Cologne, Cologne, Germany.
Technical University of Munich · DELudwig-Maximilians-Universität München · DEMax Planck Institute for Plant Breeding Research · DEUniversity Hospital Frankfurt · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMany studies examine gene expression data that has been obtained under the influence of multiple factors, such as genetic background, environmental conditions, or exposure to diseases. The interplay of multiple factors may lead to effect modification and confounding. Higher order linear regression models can account for these effects. We present a new methodology for linear model selection and apply it to microarray data of bone marrow-derived macrophages. This experiment investigates the influence of three variable factors: the genetic background of the mice from which the macrophages were obtained, Yersinia enterocolitica infection (two strains, and a mock control), and treatment/non-treatment with interferon-γ.

resultsWe set up four different linear regression models in a hierarchical order. We introduce the eruption plot as a new practical tool for model selection complementary to global testing. It visually compares the size and significance of effect estimates between two nested models. Using this methodology we were able to select the most appropriate model by keeping only relevant factors showing additional explanatory power. Application to experimental data allowed us to qualify the interaction of factors as either neutral (no interaction), alleviating (co-occurring effects are weaker than expected from the single effects), or aggravating (stronger than expected). We find a biologically meaningful gene cluster of putative C2TA target genes that appear to be co-regulated with MHC class II genes.

conclusionsWe introduced the eruption plot as a tool for visual model comparison to identify relevant higher order interactions in the analysis of expression data obtained under the influence of multiple factors. We conclude that model selection in higher order linear regression models should generally be performed for the analysis of multi-factorial microarray data.

Indexed as

Gene Expression ProfilingAnimalsBinding SitesLinear ModelsMacrophagesMiceMice, Inbred C57BLOligonucleotide Array Sequence AnalysisRegression AnalysisTranscription FactorsYersinia InfectionsTranscription Factors

Identifiers

PMID24658540
PMCPMC3962375
OpenAlexW1978527577

What OpenQuestion holds

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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.