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MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data

Gene set enrichment analysis (GSEA) is a widely used technique in transcriptomic data analysis that uses a database of predefined gene sets to rank lists of genes from microarray studies to identify significant and coordinated changes in gene expression data. While GSEA has been playing a significan...

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Detalles Bibliográficos
Autores principales: Xia, Jianguo, Wishart, David S.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896187/
https://www.ncbi.nlm.nih.gov/pubmed/20457745
http://dx.doi.org/10.1093/nar/gkq329
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author Xia, Jianguo
Wishart, David S.
author_facet Xia, Jianguo
Wishart, David S.
author_sort Xia, Jianguo
collection PubMed
description Gene set enrichment analysis (GSEA) is a widely used technique in transcriptomic data analysis that uses a database of predefined gene sets to rank lists of genes from microarray studies to identify significant and coordinated changes in gene expression data. While GSEA has been playing a significant role in understanding transcriptomic data, no similar tools are currently available for understanding metabolomic data. Here, we introduce a web-based server, called Metabolite Set Enrichment Analysis (MSEA), to help researchers identify and interpret patterns of human or mammalian metabolite concentration changes in a biologically meaningful context. Key to the development of MSEA has been the creation of a library of ∼1000 predefined metabolite sets covering various metabolic pathways, disease states, biofluids, and tissue locations. MSEA also supports user-defined or custom metabolite sets for more specialized analysis. MSEA offers three different enrichment analyses for metabolomic studies including overrepresentation analysis (ORA), single sample profiling (SSP) and quantitative enrichment analysis (QEA). ORA requires only a list of compound names, while SSP and QEA require both compound names and compound concentrations. MSEA generates easily understood graphs or tables embedded with hyperlinks to relevant pathway images and disease descriptors. For non-mammalian or more specialized metabolomic studies, MSEA allows users to provide their own metabolite sets for enrichment analysis. The MSEA server also supports conversion between metabolite common names, synonyms, and major database identifiers. MSEA has the potential to help users identify obvious as well as ‘subtle but coordinated’ changes among a group of related metabolites that may go undetected with conventional approaches. MSEA is freely available at http://www.msea.ca.
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spelling pubmed-28961872010-07-02 MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data Xia, Jianguo Wishart, David S. Nucleic Acids Res Articles Gene set enrichment analysis (GSEA) is a widely used technique in transcriptomic data analysis that uses a database of predefined gene sets to rank lists of genes from microarray studies to identify significant and coordinated changes in gene expression data. While GSEA has been playing a significant role in understanding transcriptomic data, no similar tools are currently available for understanding metabolomic data. Here, we introduce a web-based server, called Metabolite Set Enrichment Analysis (MSEA), to help researchers identify and interpret patterns of human or mammalian metabolite concentration changes in a biologically meaningful context. Key to the development of MSEA has been the creation of a library of ∼1000 predefined metabolite sets covering various metabolic pathways, disease states, biofluids, and tissue locations. MSEA also supports user-defined or custom metabolite sets for more specialized analysis. MSEA offers three different enrichment analyses for metabolomic studies including overrepresentation analysis (ORA), single sample profiling (SSP) and quantitative enrichment analysis (QEA). ORA requires only a list of compound names, while SSP and QEA require both compound names and compound concentrations. MSEA generates easily understood graphs or tables embedded with hyperlinks to relevant pathway images and disease descriptors. For non-mammalian or more specialized metabolomic studies, MSEA allows users to provide their own metabolite sets for enrichment analysis. The MSEA server also supports conversion between metabolite common names, synonyms, and major database identifiers. MSEA has the potential to help users identify obvious as well as ‘subtle but coordinated’ changes among a group of related metabolites that may go undetected with conventional approaches. MSEA is freely available at http://www.msea.ca. Oxford University Press 2010-07-01 2010-05-10 /pmc/articles/PMC2896187/ /pubmed/20457745 http://dx.doi.org/10.1093/nar/gkq329 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Xia, Jianguo
Wishart, David S.
MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data
title MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data
title_full MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data
title_fullStr MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data
title_full_unstemmed MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data
title_short MSEA: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data
title_sort msea: a web-based tool to identify biologically meaningful patterns in quantitative metabolomic data
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896187/
https://www.ncbi.nlm.nih.gov/pubmed/20457745
http://dx.doi.org/10.1093/nar/gkq329
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