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Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes
BACKGROUND: Biological pathways are important for understanding biological mechanisms. Thus, finding important pathways that underlie biological problems helps researchers to focus on the most relevant sets of genes. Pathways resemble networks with complicated structures, but most of the existing pa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443660/ https://www.ncbi.nlm.nih.gov/pubmed/22672776 http://dx.doi.org/10.1186/1752-0509-6-56 |
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author | Gu, Zuguang Liu, Jialin Cao, Kunming Zhang, Junfeng Wang, Jin |
author_facet | Gu, Zuguang Liu, Jialin Cao, Kunming Zhang, Junfeng Wang, Jin |
author_sort | Gu, Zuguang |
collection | PubMed |
description | BACKGROUND: Biological pathways are important for understanding biological mechanisms. Thus, finding important pathways that underlie biological problems helps researchers to focus on the most relevant sets of genes. Pathways resemble networks with complicated structures, but most of the existing pathway enrichment tools ignore topological information embedded within pathways, which limits their applicability. RESULTS: A systematic and extensible pathway enrichment method in which nodes are weighted by network centrality was proposed. We demonstrate how choice of pathway structure and centrality measurement, as well as the presence of key genes, affects pathway significance. We emphasize two improvements of our method over current methods. First, allowing for the diversity of genes’ characters and the difficulty of covering gene importance from all aspects, we set centrality as an optional parameter in the model. Second, nodes rather than genes form the basic unit of pathways, such that one node can be composed of several genes and one gene may reside in different nodes. By comparing our methodology to the original enrichment method using both simulation data and real-world data, we demonstrate the efficacy of our method in finding new pathways from biological perspective. CONCLUSIONS: Our method can benefit the systematic analysis of biological pathways and help to extract more meaningful information from gene expression data. The algorithm has been implemented as an R package CePa, and also a web-based version of CePa is provided. |
format | Online Article Text |
id | pubmed-3443660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34436602012-09-18 Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes Gu, Zuguang Liu, Jialin Cao, Kunming Zhang, Junfeng Wang, Jin BMC Syst Biol Methodology Article BACKGROUND: Biological pathways are important for understanding biological mechanisms. Thus, finding important pathways that underlie biological problems helps researchers to focus on the most relevant sets of genes. Pathways resemble networks with complicated structures, but most of the existing pathway enrichment tools ignore topological information embedded within pathways, which limits their applicability. RESULTS: A systematic and extensible pathway enrichment method in which nodes are weighted by network centrality was proposed. We demonstrate how choice of pathway structure and centrality measurement, as well as the presence of key genes, affects pathway significance. We emphasize two improvements of our method over current methods. First, allowing for the diversity of genes’ characters and the difficulty of covering gene importance from all aspects, we set centrality as an optional parameter in the model. Second, nodes rather than genes form the basic unit of pathways, such that one node can be composed of several genes and one gene may reside in different nodes. By comparing our methodology to the original enrichment method using both simulation data and real-world data, we demonstrate the efficacy of our method in finding new pathways from biological perspective. CONCLUSIONS: Our method can benefit the systematic analysis of biological pathways and help to extract more meaningful information from gene expression data. The algorithm has been implemented as an R package CePa, and also a web-based version of CePa is provided. BioMed Central 2012-06-06 /pmc/articles/PMC3443660/ /pubmed/22672776 http://dx.doi.org/10.1186/1752-0509-6-56 Text en Copyright ©2012 Gu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Gu, Zuguang Liu, Jialin Cao, Kunming Zhang, Junfeng Wang, Jin Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes |
title | Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes |
title_full | Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes |
title_fullStr | Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes |
title_full_unstemmed | Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes |
title_short | Centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes |
title_sort | centrality-based pathway enrichment: a systematic approach for finding significant pathways dominated by key genes |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443660/ https://www.ncbi.nlm.nih.gov/pubmed/22672776 http://dx.doi.org/10.1186/1752-0509-6-56 |
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