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A network module-based method for identifying cancer prognostic signatures
Discovering robust prognostic gene signatures as biomarkers using genomics data can be challenging. We have developed a simple but efficient method for discovering prognostic biomarkers in cancer gene expression data sets using modules derived from a highly reliable gene functional interaction netwo...
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/PMC3580410/ https://www.ncbi.nlm.nih.gov/pubmed/23228031 http://dx.doi.org/10.1186/gb-2012-13-12-r112 |
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author | Wu, Guanming Stein, Lincoln |
author_facet | Wu, Guanming Stein, Lincoln |
author_sort | Wu, Guanming |
collection | PubMed |
description | Discovering robust prognostic gene signatures as biomarkers using genomics data can be challenging. We have developed a simple but efficient method for discovering prognostic biomarkers in cancer gene expression data sets using modules derived from a highly reliable gene functional interaction network. When applied to breast cancer, we discover a novel 31-gene signature associated with patient survival. The signature replicates across 5 independent gene expression studies, and outperforms 48 published gene signatures. When applied to ovarian cancer, the algorithm identifies a 75-gene signature associated with patient survival. A Cytoscape plugin implementation of the signature discovery method is available at http://wiki.reactome.org/index.php/Reactome_FI_Cytoscape_Plugin |
format | Online Article Text |
id | pubmed-3580410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35804102013-02-26 A network module-based method for identifying cancer prognostic signatures Wu, Guanming Stein, Lincoln Genome Biol Method Discovering robust prognostic gene signatures as biomarkers using genomics data can be challenging. We have developed a simple but efficient method for discovering prognostic biomarkers in cancer gene expression data sets using modules derived from a highly reliable gene functional interaction network. When applied to breast cancer, we discover a novel 31-gene signature associated with patient survival. The signature replicates across 5 independent gene expression studies, and outperforms 48 published gene signatures. When applied to ovarian cancer, the algorithm identifies a 75-gene signature associated with patient survival. A Cytoscape plugin implementation of the signature discovery method is available at http://wiki.reactome.org/index.php/Reactome_FI_Cytoscape_Plugin BioMed Central 2012 2012-12-10 /pmc/articles/PMC3580410/ /pubmed/23228031 http://dx.doi.org/10.1186/gb-2012-13-12-r112 Text en Copyright ©2012 Wu and Stein; 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 | Method Wu, Guanming Stein, Lincoln A network module-based method for identifying cancer prognostic signatures |
title | A network module-based method for identifying cancer prognostic signatures |
title_full | A network module-based method for identifying cancer prognostic signatures |
title_fullStr | A network module-based method for identifying cancer prognostic signatures |
title_full_unstemmed | A network module-based method for identifying cancer prognostic signatures |
title_short | A network module-based method for identifying cancer prognostic signatures |
title_sort | network module-based method for identifying cancer prognostic signatures |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580410/ https://www.ncbi.nlm.nih.gov/pubmed/23228031 http://dx.doi.org/10.1186/gb-2012-13-12-r112 |
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