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PathNet: a tool for pathway analysis using topological information
BACKGROUND: Identification of canonical pathways through enrichment of differentially expressed genes in a given pathway is a widely used method for interpreting gene lists generated from high-throughput experimental studies. However, most algorithms treat pathways as sets of genes, disregarding any...
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/PMC3563509/ https://www.ncbi.nlm.nih.gov/pubmed/23006764 http://dx.doi.org/10.1186/1751-0473-7-10 |
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author | Dutta, Bhaskar Wallqvist, Anders Reifman, Jaques |
author_facet | Dutta, Bhaskar Wallqvist, Anders Reifman, Jaques |
author_sort | Dutta, Bhaskar |
collection | PubMed |
description | BACKGROUND: Identification of canonical pathways through enrichment of differentially expressed genes in a given pathway is a widely used method for interpreting gene lists generated from high-throughput experimental studies. However, most algorithms treat pathways as sets of genes, disregarding any inter- and intra-pathway connectivity information, and do not provide insights beyond identifying lists of pathways. RESULTS: We developed an algorithm (PathNet) that utilizes the connectivity information in canonical pathway descriptions to help identify study-relevant pathways and characterize non-obvious dependencies and connections among pathways using gene expression data. PathNet considers both the differential expression of genes and their pathway neighbors to strengthen the evidence that a pathway is implicated in the biological conditions characterizing the experiment. As an adjunct to this analysis, PathNet uses the connectivity of the differentially expressed genes among all pathways to score pathway contextual associations and statistically identify biological relations among pathways. In this study, we used PathNet to identify biologically relevant results in two Alzheimer’s disease microarray datasets, and compared its performance with existing methods. Importantly, PathNet identified de-regulation of the ubiquitin-mediated proteolysis pathway as an important component in Alzheimer’s disease progression, despite the absence of this pathway in the standard enrichment analyses. CONCLUSIONS: PathNet is a novel method for identifying enrichment and association between canonical pathways in the context of gene expression data. It takes into account topological information present in pathways to reveal biological information. PathNet is available as an R workspace image from http://www.bhsai.org/downloads/pathnet/. |
format | Online Article Text |
id | pubmed-3563509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35635092013-02-08 PathNet: a tool for pathway analysis using topological information Dutta, Bhaskar Wallqvist, Anders Reifman, Jaques Source Code Biol Med Research BACKGROUND: Identification of canonical pathways through enrichment of differentially expressed genes in a given pathway is a widely used method for interpreting gene lists generated from high-throughput experimental studies. However, most algorithms treat pathways as sets of genes, disregarding any inter- and intra-pathway connectivity information, and do not provide insights beyond identifying lists of pathways. RESULTS: We developed an algorithm (PathNet) that utilizes the connectivity information in canonical pathway descriptions to help identify study-relevant pathways and characterize non-obvious dependencies and connections among pathways using gene expression data. PathNet considers both the differential expression of genes and their pathway neighbors to strengthen the evidence that a pathway is implicated in the biological conditions characterizing the experiment. As an adjunct to this analysis, PathNet uses the connectivity of the differentially expressed genes among all pathways to score pathway contextual associations and statistically identify biological relations among pathways. In this study, we used PathNet to identify biologically relevant results in two Alzheimer’s disease microarray datasets, and compared its performance with existing methods. Importantly, PathNet identified de-regulation of the ubiquitin-mediated proteolysis pathway as an important component in Alzheimer’s disease progression, despite the absence of this pathway in the standard enrichment analyses. CONCLUSIONS: PathNet is a novel method for identifying enrichment and association between canonical pathways in the context of gene expression data. It takes into account topological information present in pathways to reveal biological information. PathNet is available as an R workspace image from http://www.bhsai.org/downloads/pathnet/. BioMed Central 2012-09-24 /pmc/articles/PMC3563509/ /pubmed/23006764 http://dx.doi.org/10.1186/1751-0473-7-10 Text en Copyright ©2012 Dutta 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 | Research Dutta, Bhaskar Wallqvist, Anders Reifman, Jaques PathNet: a tool for pathway analysis using topological information |
title | PathNet: a tool for pathway analysis using topological information |
title_full | PathNet: a tool for pathway analysis using topological information |
title_fullStr | PathNet: a tool for pathway analysis using topological information |
title_full_unstemmed | PathNet: a tool for pathway analysis using topological information |
title_short | PathNet: a tool for pathway analysis using topological information |
title_sort | pathnet: a tool for pathway analysis using topological information |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563509/ https://www.ncbi.nlm.nih.gov/pubmed/23006764 http://dx.doi.org/10.1186/1751-0473-7-10 |
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