Evidence map›Paper›PMID 19574285›Full record

ArticleBioinformatics (Oxford, England)2009

Unite and conquer: univariate and multivariate approaches for finding differentially expressed gene sets.

Galina V Glazko, Frank Emmert-Streib

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

60 citing papers in PubMed.

  1. Article
  2. A practical guide to functional enrichment analysis.Frontiers in bioinformatics · 2026
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  4. Review
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  15. Article
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  18. Crosstalk analysis of dysregulated pathways in preeclampsia.Experimental and therapeutic medicine · 2019
    Article
  19. Article
  20. 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

2 authors.

Galina V GlazkoDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, NY 14642, USA. Galina_Glazko@urmc.rochester.edu
Frank Emmert-Streib

Funding

Correlation Vectors in Gene Expression ProfilingR21GM079259 · NIGMS · UNIVERSITY OF ROCHESTER · PI QIU, XING · 2007 to 2008
$424k
Novel methods of hypothesis testing for pathway recognition in genomic dataR21HG004648 · NHGRI · UNIVERSITY OF ROCHESTER · PI ALMUDEVAR, ANTHONY · 2008 to 2009
$424k
NHGRI NIH HHS R21 HG004648NHGRI NIH HHS R21HG004648NIGMS NIH HHS GM079259NIGMS NIH HHS R21 GM079259
6 · The paper itself

Abstract

motivationRecently, many univariate and several multivariate approaches have been suggested for testing differential expression of gene sets between different phenotypes. However, despite a wealth of literature studying their performance on simulated and real biological data, still there is a need to quantify their relative performance when they are testing different null hypotheses.

resultsIn this article, we compare the performance of univariate and multivariate tests on both simulated and biological data. In the simulation study we demonstrate that high correlations equally affect the power of both, univariate as well as multivariate tests. In addition, for most of them the power is similarly affected by the dimensionality of the gene set and by the percentage of genes in the set, for which expression is changing between two phenotypes. The application of different test statistics to biological data reveals that three statistics (sum of squared t-tests, Hotelling's T(2), N-statistic), testing different null hypotheses, find some common but also some complementing differentially expressed gene sets under specific settings. This demonstrates that due to complementing null hypotheses each test projects on different aspects of the data and for the analysis of biological data it is beneficial to use all three tests simultaneously instead of focusing exclusively on just one.

Indexed as

Gene Expression ProfilingComputational BiologyHumansModels, StatisticalOligonucleotide Array Sequence AnalysisPhenotype

Identifiers

PMID19574285
PMCPMC2735665

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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.