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PathFinder: mining signal transduction pathway segments from protein-protein interaction networks
BACKGROUND: A Signal transduction pathway is the chain of processes by which a cell converts an extracellular signal into a response. In most unicellular organisms, the number of signal transduction pathways influences the number of ways the cell can react and respond to the environment. Discovering...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2100073/ https://www.ncbi.nlm.nih.gov/pubmed/17854489 http://dx.doi.org/10.1186/1471-2105-8-335 |
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author | Bebek, Gurkan Yang, Jiong |
author_facet | Bebek, Gurkan Yang, Jiong |
author_sort | Bebek, Gurkan |
collection | PubMed |
description | BACKGROUND: A Signal transduction pathway is the chain of processes by which a cell converts an extracellular signal into a response. In most unicellular organisms, the number of signal transduction pathways influences the number of ways the cell can react and respond to the environment. Discovering signal transduction pathways is an arduous problem, even with the use of systematic genomic, proteomic and metabolomic technologies. These techniques lead to an enormous amount of data and how to interpret and process this data becomes a challenging computational problem. RESULTS: In this study we present a new framework for identifying signaling pathways in protein-protein interaction networks. Our goal is to find biologically significant pathway segments in a given interaction network. Currently, protein-protein interaction data has excessive amount of noise, e.g., false positive and false negative interactions. First, we eliminate false positives in the protein-protein interaction network by integrating the network with microarray expression profiles, protein subcellular localization and sequence information. In addition, protein families are used to repair false negative interactions. Then the characteristics of known signal transduction pathways and their functional annotations are extracted in the form of association rules. CONCLUSION: Given a pair of starting and ending proteins, our methodology returns candidate pathway segments between these two proteins with possible missing links (recovered false negatives). In our study, S. cerevisiae (yeast) data is used to demonstrate the effectiveness of our method. |
format | Text |
id | pubmed-2100073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-21000732007-12-03 PathFinder: mining signal transduction pathway segments from protein-protein interaction networks Bebek, Gurkan Yang, Jiong BMC Bioinformatics Research Article BACKGROUND: A Signal transduction pathway is the chain of processes by which a cell converts an extracellular signal into a response. In most unicellular organisms, the number of signal transduction pathways influences the number of ways the cell can react and respond to the environment. Discovering signal transduction pathways is an arduous problem, even with the use of systematic genomic, proteomic and metabolomic technologies. These techniques lead to an enormous amount of data and how to interpret and process this data becomes a challenging computational problem. RESULTS: In this study we present a new framework for identifying signaling pathways in protein-protein interaction networks. Our goal is to find biologically significant pathway segments in a given interaction network. Currently, protein-protein interaction data has excessive amount of noise, e.g., false positive and false negative interactions. First, we eliminate false positives in the protein-protein interaction network by integrating the network with microarray expression profiles, protein subcellular localization and sequence information. In addition, protein families are used to repair false negative interactions. Then the characteristics of known signal transduction pathways and their functional annotations are extracted in the form of association rules. CONCLUSION: Given a pair of starting and ending proteins, our methodology returns candidate pathway segments between these two proteins with possible missing links (recovered false negatives). In our study, S. cerevisiae (yeast) data is used to demonstrate the effectiveness of our method. BioMed Central 2007-09-13 /pmc/articles/PMC2100073/ /pubmed/17854489 http://dx.doi.org/10.1186/1471-2105-8-335 Text en Copyright © 2007 Bebek and Yang; 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 Article Bebek, Gurkan Yang, Jiong PathFinder: mining signal transduction pathway segments from protein-protein interaction networks |
title | PathFinder: mining signal transduction pathway segments from protein-protein interaction networks |
title_full | PathFinder: mining signal transduction pathway segments from protein-protein interaction networks |
title_fullStr | PathFinder: mining signal transduction pathway segments from protein-protein interaction networks |
title_full_unstemmed | PathFinder: mining signal transduction pathway segments from protein-protein interaction networks |
title_short | PathFinder: mining signal transduction pathway segments from protein-protein interaction networks |
title_sort | pathfinder: mining signal transduction pathway segments from protein-protein interaction networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2100073/ https://www.ncbi.nlm.nih.gov/pubmed/17854489 http://dx.doi.org/10.1186/1471-2105-8-335 |
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