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Along signal paths: an empirical gene set approach exploiting pathway topology
Gene set analysis using biological pathways has become a widely used statistical approach for gene expression analysis. A biological pathway can be represented through a graph where genes and their interactions are, respectively, nodes and edges of the graph. From a biological point of view only som...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592432/ https://www.ncbi.nlm.nih.gov/pubmed/23002139 http://dx.doi.org/10.1093/nar/gks866 |
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author | Martini, Paolo Sales, Gabriele Massa, M. Sofia Chiogna, Monica Romualdi, Chiara |
author_facet | Martini, Paolo Sales, Gabriele Massa, M. Sofia Chiogna, Monica Romualdi, Chiara |
author_sort | Martini, Paolo |
collection | PubMed |
description | Gene set analysis using biological pathways has become a widely used statistical approach for gene expression analysis. A biological pathway can be represented through a graph where genes and their interactions are, respectively, nodes and edges of the graph. From a biological point of view only some portions of a pathway are expected to be altered; however, few methods using pathway topology have been proposed and none of them tries to identify the signal paths, within a pathway, mostly involved in the biological problem. Here, we present a novel algorithm for pathway analysis clipper, that tries to fill in this gap. clipper implements a two-step empirical approach based on the exploitation of graph decomposition into a junction tree to reconstruct the most relevant signal path. In the first step clipper selects significant pathways according to statistical tests on the means and the concentration matrices of the graphs derived from pathway topologies. Then, it identifies within these pathways the signal paths having the greatest association with a specific phenotype. We test our approach on simulated and two real expression datasets. Our results demonstrate the efficacy of clipper in the identification of signal transduction paths totally coherent with the biological problem. |
format | Online Article Text |
id | pubmed-3592432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35924322013-03-08 Along signal paths: an empirical gene set approach exploiting pathway topology Martini, Paolo Sales, Gabriele Massa, M. Sofia Chiogna, Monica Romualdi, Chiara Nucleic Acids Res Methods Online Gene set analysis using biological pathways has become a widely used statistical approach for gene expression analysis. A biological pathway can be represented through a graph where genes and their interactions are, respectively, nodes and edges of the graph. From a biological point of view only some portions of a pathway are expected to be altered; however, few methods using pathway topology have been proposed and none of them tries to identify the signal paths, within a pathway, mostly involved in the biological problem. Here, we present a novel algorithm for pathway analysis clipper, that tries to fill in this gap. clipper implements a two-step empirical approach based on the exploitation of graph decomposition into a junction tree to reconstruct the most relevant signal path. In the first step clipper selects significant pathways according to statistical tests on the means and the concentration matrices of the graphs derived from pathway topologies. Then, it identifies within these pathways the signal paths having the greatest association with a specific phenotype. We test our approach on simulated and two real expression datasets. Our results demonstrate the efficacy of clipper in the identification of signal transduction paths totally coherent with the biological problem. Oxford University Press 2013-01 2012-09-21 /pmc/articles/PMC3592432/ /pubmed/23002139 http://dx.doi.org/10.1093/nar/gks866 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Martini, Paolo Sales, Gabriele Massa, M. Sofia Chiogna, Monica Romualdi, Chiara Along signal paths: an empirical gene set approach exploiting pathway topology |
title | Along signal paths: an empirical gene set approach exploiting pathway topology |
title_full | Along signal paths: an empirical gene set approach exploiting pathway topology |
title_fullStr | Along signal paths: an empirical gene set approach exploiting pathway topology |
title_full_unstemmed | Along signal paths: an empirical gene set approach exploiting pathway topology |
title_short | Along signal paths: an empirical gene set approach exploiting pathway topology |
title_sort | along signal paths: an empirical gene set approach exploiting pathway topology |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592432/ https://www.ncbi.nlm.nih.gov/pubmed/23002139 http://dx.doi.org/10.1093/nar/gks866 |
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