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Down-weighting overlapping genes improves gene set analysis
BACKGROUND: The identification of gene sets that are significantly impacted in a given condition based on microarray data is a crucial step in current life science research. Most gene set analysis methods treat genes equally, regardless how specific they are to a given gene set. RESULTS: In this wor...
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/PMC3443069/ https://www.ncbi.nlm.nih.gov/pubmed/22713124 http://dx.doi.org/10.1186/1471-2105-13-136 |
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author | Tarca, Adi Laurentiu Draghici, Sorin Bhatti, Gaurav Romero, Roberto |
author_facet | Tarca, Adi Laurentiu Draghici, Sorin Bhatti, Gaurav Romero, Roberto |
author_sort | Tarca, Adi Laurentiu |
collection | PubMed |
description | BACKGROUND: The identification of gene sets that are significantly impacted in a given condition based on microarray data is a crucial step in current life science research. Most gene set analysis methods treat genes equally, regardless how specific they are to a given gene set. RESULTS: In this work we propose a new gene set analysis method that computes a gene set score as the mean of absolute values of weighted moderated gene t-scores. The gene weights are designed to emphasize the genes appearing in few gene sets, versus genes that appear in many gene sets. We demonstrate the usefulness of the method when analyzing gene sets that correspond to the KEGG pathways, and hence we called our method Pathway Analysis with Down-weighting of Overlapping Genes (PADOG). Unlike most gene set analysis methods which are validated through the analysis of 2-3 data sets followed by a human interpretation of the results, the validation employed here uses 24 different data sets and a completely objective assessment scheme that makes minimal assumptions and eliminates the need for possibly biased human assessments of the analysis results. CONCLUSIONS: PADOG significantly improves gene set ranking and boosts sensitivity of analysis using information already available in the gene expression profiles and the collection of gene sets to be analyzed. The advantages of PADOG over other existing approaches are shown to be stable to changes in the database of gene sets to be analyzed. PADOG was implemented as an R package available at: http://bioinformaticsprb.med.wayne.edu/PADOG/or http://www.bioconductor.org. |
format | Online Article Text |
id | pubmed-3443069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34430692012-09-18 Down-weighting overlapping genes improves gene set analysis Tarca, Adi Laurentiu Draghici, Sorin Bhatti, Gaurav Romero, Roberto BMC Bioinformatics Research Article BACKGROUND: The identification of gene sets that are significantly impacted in a given condition based on microarray data is a crucial step in current life science research. Most gene set analysis methods treat genes equally, regardless how specific they are to a given gene set. RESULTS: In this work we propose a new gene set analysis method that computes a gene set score as the mean of absolute values of weighted moderated gene t-scores. The gene weights are designed to emphasize the genes appearing in few gene sets, versus genes that appear in many gene sets. We demonstrate the usefulness of the method when analyzing gene sets that correspond to the KEGG pathways, and hence we called our method Pathway Analysis with Down-weighting of Overlapping Genes (PADOG). Unlike most gene set analysis methods which are validated through the analysis of 2-3 data sets followed by a human interpretation of the results, the validation employed here uses 24 different data sets and a completely objective assessment scheme that makes minimal assumptions and eliminates the need for possibly biased human assessments of the analysis results. CONCLUSIONS: PADOG significantly improves gene set ranking and boosts sensitivity of analysis using information already available in the gene expression profiles and the collection of gene sets to be analyzed. The advantages of PADOG over other existing approaches are shown to be stable to changes in the database of gene sets to be analyzed. PADOG was implemented as an R package available at: http://bioinformaticsprb.med.wayne.edu/PADOG/or http://www.bioconductor.org. BioMed Central 2012-06-19 /pmc/articles/PMC3443069/ /pubmed/22713124 http://dx.doi.org/10.1186/1471-2105-13-136 Text en Copyright ©2012 Tarca 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 Article Tarca, Adi Laurentiu Draghici, Sorin Bhatti, Gaurav Romero, Roberto Down-weighting overlapping genes improves gene set analysis |
title | Down-weighting overlapping genes improves gene set analysis |
title_full | Down-weighting overlapping genes improves gene set analysis |
title_fullStr | Down-weighting overlapping genes improves gene set analysis |
title_full_unstemmed | Down-weighting overlapping genes improves gene set analysis |
title_short | Down-weighting overlapping genes improves gene set analysis |
title_sort | down-weighting overlapping genes improves gene set analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443069/ https://www.ncbi.nlm.nih.gov/pubmed/22713124 http://dx.doi.org/10.1186/1471-2105-13-136 |
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