Evidence map›Paper›PMID 21685094›Full record

ArticleBioinformatics (Oxford, England)2011

From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems.

Ludwig Geistlinger, Gergely Csaba, Robert Küffner, Nicola Mulder, Ralf Zimmer

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Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

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33citing papers in PubMed
–field-weighted citation impact
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3 · Its place in the literature

Who cites it

33 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ludwig GeistlingerInstitute for Informatics, Ludwig-Maximilians-Universität Münchchen, Amalienstrasse 17, 80333 München, Germany. Ludwig.Geistlinger@bio.ifi.lmu.de
Gergely Csaba
Robert Küffner
Nicola Mulder
Ralf Zimmer

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationCurrent gene set enrichment approaches do not take interactions and associations between set members into account. Mutual activation and inhibition causing positive and negative correlation among set members are thus neglected. As a consequence, inconsistent regulations and contextless expression changes are reported and, thus, the biological interpretation of the result is impeded.

resultsWe analyzed established gene set enrichment methods and their result sets in a large-scale investigation of 1000 expression datasets. The reported statistically significant gene sets exhibit only average consistency between the observed patterns of differential expression and known regulatory interactions. We present Gene Graph Enrichment Analysis (GGEA) to detect consistently and coherently enriched gene sets, based on prior knowledge derived from directed gene regulatory networks. Firstly, GGEA improves the concordance of pairwise regulation with individual expression changes in respective pairs of regulating and regulated genes, compared with set enrichment methods. Secondly, GGEA yields result sets where a large fraction of relevant expression changes can be explained by nearby regulators, such as transcription factors, again improving on set-based methods. Thirdly, we demonstrate in additional case studies that GGEA can be applied to human regulatory pathways, where it sensitively detects very specific regulation processes, which are altered in tumors of the central nervous system. GGEA significantly increases the detection of gene sets where measured positively or negatively correlated expression patterns coincide with directed inducing or repressing relationships, thus facilitating further interpretation of gene expression data. AVAILABILITY: The method and accompanying visualization capabilities have been bundled into an R package and tied to a grahical user interface, the Galaxy workflow environment, that is running as a web server. CONTACT: Ludwig.Geistlinger@bio.ifi.lmu.de; Ralf.Zimmer@bio.ifi.lmu.de.

Indexed as

Gene Expression ProfilingSoftwareAlgorithmsGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansNeoplasms, Nerve TissueProteinsSignal TransductionProteins

Identifiers

PMID21685094
PMCPMC3117393

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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.