Cargando…

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

Motivation: Current 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 e...

Descripción completa

Detalles Bibliográficos
Autores principales: Geistlinger, Ludwig, Csaba, Gergely, Küffner, Robert, Mulder, Nicola, Zimmer, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117393/
https://www.ncbi.nlm.nih.gov/pubmed/21685094
http://dx.doi.org/10.1093/bioinformatics/btr228
_version_ 1782206328388714496
author Geistlinger, Ludwig
Csaba, Gergely
Küffner, Robert
Mulder, Nicola
Zimmer, Ralf
author_facet Geistlinger, Ludwig
Csaba, Gergely
Küffner, Robert
Mulder, Nicola
Zimmer, Ralf
author_sort Geistlinger, Ludwig
collection PubMed
description Motivation: Current 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. Results: We 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
format Online
Article
Text
id pubmed-3117393
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-31173932011-06-17 From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems Geistlinger, Ludwig Csaba, Gergely Küffner, Robert Mulder, Nicola Zimmer, Ralf Bioinformatics Ismb/Eccb 2011 Proceedings Papers Committee July 17 to July 19, 2011, Vienna, Austria Motivation: Current 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. Results: We 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 Oxford University Press 2011-07-01 2011-06-14 /pmc/articles/PMC3117393/ /pubmed/21685094 http://dx.doi.org/10.1093/bioinformatics/btr228 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Ismb/Eccb 2011 Proceedings Papers Committee July 17 to July 19, 2011, Vienna, Austria
Geistlinger, Ludwig
Csaba, Gergely
Küffner, Robert
Mulder, Nicola
Zimmer, Ralf
From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems
title From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems
title_full From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems
title_fullStr From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems
title_full_unstemmed From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems
title_short From sets to graphs: towards a realistic enrichment analysis of transcriptomic systems
title_sort from sets to graphs: towards a realistic enrichment analysis of transcriptomic systems
topic Ismb/Eccb 2011 Proceedings Papers Committee July 17 to July 19, 2011, Vienna, Austria
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117393/
https://www.ncbi.nlm.nih.gov/pubmed/21685094
http://dx.doi.org/10.1093/bioinformatics/btr228
work_keys_str_mv AT geistlingerludwig fromsetstographstowardsarealisticenrichmentanalysisoftranscriptomicsystems
AT csabagergely fromsetstographstowardsarealisticenrichmentanalysisoftranscriptomicsystems
AT kuffnerrobert fromsetstographstowardsarealisticenrichmentanalysisoftranscriptomicsystems
AT muldernicola fromsetstographstowardsarealisticenrichmentanalysisoftranscriptomicsystems
AT zimmerralf fromsetstographstowardsarealisticenrichmentanalysisoftranscriptomicsystems