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IDSL.GOA: Gene Ontology Analysis for Metabolomics

Biological interpretation of metabolomics datasets often ends at a pathway analysis step to find the over-represented metabolic pathways in the list of statistically significant metabolites. However, definitions of biochemical pathways and metabolite coverage vary among different curated databases,...

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Autores principales: Mahajan, Priyanka, Fiehn, Oliver, Barupal, Dinesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081191/
https://www.ncbi.nlm.nih.gov/pubmed/37034715
http://dx.doi.org/10.1101/2023.03.25.534225
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author Mahajan, Priyanka
Fiehn, Oliver
Barupal, Dinesh
author_facet Mahajan, Priyanka
Fiehn, Oliver
Barupal, Dinesh
author_sort Mahajan, Priyanka
collection PubMed
description Biological interpretation of metabolomics datasets often ends at a pathway analysis step to find the over-represented metabolic pathways in the list of statistically significant metabolites. However, definitions of biochemical pathways and metabolite coverage vary among different curated databases, leading to inaccurate and contradicting interpretations. For the lists of gene, transcripts and proteins, Gene Ontology (GO) terms over-presentation analysis has become a standardized approach for the biological interpretation. But, GO analysis has not been achieved for metabolomics datasets. We present a new knowledgebase and the online tool, Gene Ontology Analysis by the Integrated Data Science Laboratory for Metabolomics and Exposomics (IDSL.GOA) to conduct GO over-representation analysis for a metabolite list. The IDSL.GOA knowledgebase covers 2,324 metabolic GO terms and associated 2,818 genes, 22,264 transcripts, 20,158 proteins, 1,482 EC annotations, 2,430 reactions and 2,212 metabolites. IDSL.GOA analysis of a case study of older vs young female brain cortex metabolome highlighted over 250 GO terms being significantly overrepresented (FDR <0.05). On contrast, for the same metabolite list, MetaboAnalyst and Reactome Pathway Analysis suggested less than 5 pathways at FDR <0.05. We showed how IDSL.GOA identified key and relevant GO metabolic processes that were not mentioned by alternative pathway analysis approaches. Overall, we suggest that metabolomics researchers should not limit the interpretation of metabolite lists to only pathway maps and can also leverage GO terms as well. IDSL.GOA provides a powerful tool for this purpose, allowing for a more comprehensive and accurate analysis of metabolite pathway data. IDSL.GOA tool can be accessed at https://goa.idsl.me/
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spelling pubmed-100811912023-04-08 IDSL.GOA: Gene Ontology Analysis for Metabolomics Mahajan, Priyanka Fiehn, Oliver Barupal, Dinesh bioRxiv Article Biological interpretation of metabolomics datasets often ends at a pathway analysis step to find the over-represented metabolic pathways in the list of statistically significant metabolites. However, definitions of biochemical pathways and metabolite coverage vary among different curated databases, leading to inaccurate and contradicting interpretations. For the lists of gene, transcripts and proteins, Gene Ontology (GO) terms over-presentation analysis has become a standardized approach for the biological interpretation. But, GO analysis has not been achieved for metabolomics datasets. We present a new knowledgebase and the online tool, Gene Ontology Analysis by the Integrated Data Science Laboratory for Metabolomics and Exposomics (IDSL.GOA) to conduct GO over-representation analysis for a metabolite list. The IDSL.GOA knowledgebase covers 2,324 metabolic GO terms and associated 2,818 genes, 22,264 transcripts, 20,158 proteins, 1,482 EC annotations, 2,430 reactions and 2,212 metabolites. IDSL.GOA analysis of a case study of older vs young female brain cortex metabolome highlighted over 250 GO terms being significantly overrepresented (FDR <0.05). On contrast, for the same metabolite list, MetaboAnalyst and Reactome Pathway Analysis suggested less than 5 pathways at FDR <0.05. We showed how IDSL.GOA identified key and relevant GO metabolic processes that were not mentioned by alternative pathway analysis approaches. Overall, we suggest that metabolomics researchers should not limit the interpretation of metabolite lists to only pathway maps and can also leverage GO terms as well. IDSL.GOA provides a powerful tool for this purpose, allowing for a more comprehensive and accurate analysis of metabolite pathway data. IDSL.GOA tool can be accessed at https://goa.idsl.me/ Cold Spring Harbor Laboratory 2023-07-03 /pmc/articles/PMC10081191/ /pubmed/37034715 http://dx.doi.org/10.1101/2023.03.25.534225 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Mahajan, Priyanka
Fiehn, Oliver
Barupal, Dinesh
IDSL.GOA: Gene Ontology Analysis for Metabolomics
title IDSL.GOA: Gene Ontology Analysis for Metabolomics
title_full IDSL.GOA: Gene Ontology Analysis for Metabolomics
title_fullStr IDSL.GOA: Gene Ontology Analysis for Metabolomics
title_full_unstemmed IDSL.GOA: Gene Ontology Analysis for Metabolomics
title_short IDSL.GOA: Gene Ontology Analysis for Metabolomics
title_sort idsl.goa: gene ontology analysis for metabolomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10081191/
https://www.ncbi.nlm.nih.gov/pubmed/37034715
http://dx.doi.org/10.1101/2023.03.25.534225
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