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The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems

BACKGROUND: The Gene Ontology (GO) is used to describe genes and gene products from many organisms. When used for functional annotation of microarray data, GO is often slimmed by editing so that only higher level terms remain. This practice is designed to improve the summarizing of experimental resu...

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Autores principales: Geifman, Nophar, Monsonego, Alon, Rubin, Eitan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949890/
https://www.ncbi.nlm.nih.gov/pubmed/20831831
http://dx.doi.org/10.1186/1471-2105-11-458
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author Geifman, Nophar
Monsonego, Alon
Rubin, Eitan
author_facet Geifman, Nophar
Monsonego, Alon
Rubin, Eitan
author_sort Geifman, Nophar
collection PubMed
description BACKGROUND: The Gene Ontology (GO) is used to describe genes and gene products from many organisms. When used for functional annotation of microarray data, GO is often slimmed by editing so that only higher level terms remain. This practice is designed to improve the summarizing of experimental results by grouping high level terms and the statistical power of GO term enrichment analysis. Here, we propose a new approach to editing the gene ontology, clipping, which is the editing of GO according to biological relevance. Creation of a GO subset by clipping is achieved by removing terms (from all hierarchal levels) if they are not functionally relevant to a given domain of interest. Terms that are located in levels higher to relevant terms are kept, thus, biologically irrelevant terms are only removed if they are not parental to terms that are relevant. RESULTS: Using this approach, we have created the Neural-Immune Gene Ontology (NIGO) subset of GO directed for neurological and immunological systems. We tested the performance of NIGO in extracting knowledge from microarray experiments by conducting functional analysis and comparing the results to those obtained using the full GO and a generic GO slim. NIGO not only improved the statistical scores given to relevant terms, but was also able to retrieve functionally relevant terms that did not pass statistical cutoffs when using the full GO or the slim subset. CONCLUSIONS: Our results validate the pipeline used to generate NIGO, suggesting it is indeed enriched with terms that are specific to the neural/immune domains. The results suggest that NIGO can enhance the analysis of microarray experiments involving neural and/or immune related systems. They also directly demonstrate the potential such a domain-specific GO has in generating meaningful hypotheses.
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spelling pubmed-29498902010-10-06 The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems Geifman, Nophar Monsonego, Alon Rubin, Eitan BMC Bioinformatics Research Article BACKGROUND: The Gene Ontology (GO) is used to describe genes and gene products from many organisms. When used for functional annotation of microarray data, GO is often slimmed by editing so that only higher level terms remain. This practice is designed to improve the summarizing of experimental results by grouping high level terms and the statistical power of GO term enrichment analysis. Here, we propose a new approach to editing the gene ontology, clipping, which is the editing of GO according to biological relevance. Creation of a GO subset by clipping is achieved by removing terms (from all hierarchal levels) if they are not functionally relevant to a given domain of interest. Terms that are located in levels higher to relevant terms are kept, thus, biologically irrelevant terms are only removed if they are not parental to terms that are relevant. RESULTS: Using this approach, we have created the Neural-Immune Gene Ontology (NIGO) subset of GO directed for neurological and immunological systems. We tested the performance of NIGO in extracting knowledge from microarray experiments by conducting functional analysis and comparing the results to those obtained using the full GO and a generic GO slim. NIGO not only improved the statistical scores given to relevant terms, but was also able to retrieve functionally relevant terms that did not pass statistical cutoffs when using the full GO or the slim subset. CONCLUSIONS: Our results validate the pipeline used to generate NIGO, suggesting it is indeed enriched with terms that are specific to the neural/immune domains. The results suggest that NIGO can enhance the analysis of microarray experiments involving neural and/or immune related systems. They also directly demonstrate the potential such a domain-specific GO has in generating meaningful hypotheses. BioMed Central 2010-09-12 /pmc/articles/PMC2949890/ /pubmed/20831831 http://dx.doi.org/10.1186/1471-2105-11-458 Text en Copyright ©2010 Geifman 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
Geifman, Nophar
Monsonego, Alon
Rubin, Eitan
The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems
title The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems
title_full The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems
title_fullStr The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems
title_full_unstemmed The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems
title_short The Neural/Immune Gene Ontology: clipping the Gene Ontology for neurological and immunological systems
title_sort neural/immune gene ontology: clipping the gene ontology for neurological and immunological systems
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949890/
https://www.ncbi.nlm.nih.gov/pubmed/20831831
http://dx.doi.org/10.1186/1471-2105-11-458
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