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ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis

Pathway analyses are key methods to analyze 'omics experiments. Nevertheless, integrating data from different 'omics technologies and different species still requires considerable bioinformatics knowledge. Here we present the novel ReactomeGSA resource for comparative pathway analyses of m...

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Autores principales: Griss, Johannes, Viteri, Guilherme, Sidiropoulos, Konstantinos, Nguyen, Vy, Fabregat, Antonio, Hermjakob, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Biochemistry and Molecular Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710148/
https://www.ncbi.nlm.nih.gov/pubmed/32907876
http://dx.doi.org/10.1074/mcp.TIR120.002155
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author Griss, Johannes
Viteri, Guilherme
Sidiropoulos, Konstantinos
Nguyen, Vy
Fabregat, Antonio
Hermjakob, Henning
author_facet Griss, Johannes
Viteri, Guilherme
Sidiropoulos, Konstantinos
Nguyen, Vy
Fabregat, Antonio
Hermjakob, Henning
author_sort Griss, Johannes
collection PubMed
description Pathway analyses are key methods to analyze 'omics experiments. Nevertheless, integrating data from different 'omics technologies and different species still requires considerable bioinformatics knowledge. Here we present the novel ReactomeGSA resource for comparative pathway analyses of multi-omics datasets. ReactomeGSA can be used through Reactome's existing web interface and the novel ReactomeGSA R Bioconductor package with explicit support for scRNA-seq data. Data from different species is automatically mapped to a common pathway space. Public data from ExpressionAtlas and Single Cell ExpressionAtlas can be directly integrated in the analysis. ReactomeGSA greatly reduces the technical barrier for multi-omics, cross-species, comparative pathway analyses. We used ReactomeGSA to characterize the role of B cells in anti-tumor immunity. We compared B cell rich and poor human cancer samples from five of the Cancer Genome Atlas (TCGA) transcriptomics and two of the Clinical Proteomic Tumor Analysis Consortium (CPTAC) proteomics studies. B cell-rich lung adenocarcinoma samples lacked the otherwise present activation through NFkappaB. This may be linked to the presence of a specific subset of tumor associated IgG+ plasma cells that lack NFkappaB activation in scRNA-seq data from human melanoma. This showcases how ReactomeGSA can derive novel biomedical insights by integrating large multi-omics datasets.
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spelling pubmed-77101482020-12-08 ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis Griss, Johannes Viteri, Guilherme Sidiropoulos, Konstantinos Nguyen, Vy Fabregat, Antonio Hermjakob, Henning Mol Cell Proteomics Technological Innovation and Resources Pathway analyses are key methods to analyze 'omics experiments. Nevertheless, integrating data from different 'omics technologies and different species still requires considerable bioinformatics knowledge. Here we present the novel ReactomeGSA resource for comparative pathway analyses of multi-omics datasets. ReactomeGSA can be used through Reactome's existing web interface and the novel ReactomeGSA R Bioconductor package with explicit support for scRNA-seq data. Data from different species is automatically mapped to a common pathway space. Public data from ExpressionAtlas and Single Cell ExpressionAtlas can be directly integrated in the analysis. ReactomeGSA greatly reduces the technical barrier for multi-omics, cross-species, comparative pathway analyses. We used ReactomeGSA to characterize the role of B cells in anti-tumor immunity. We compared B cell rich and poor human cancer samples from five of the Cancer Genome Atlas (TCGA) transcriptomics and two of the Clinical Proteomic Tumor Analysis Consortium (CPTAC) proteomics studies. B cell-rich lung adenocarcinoma samples lacked the otherwise present activation through NFkappaB. This may be linked to the presence of a specific subset of tumor associated IgG+ plasma cells that lack NFkappaB activation in scRNA-seq data from human melanoma. This showcases how ReactomeGSA can derive novel biomedical insights by integrating large multi-omics datasets. The American Society for Biochemistry and Molecular Biology 2020-12 2020-09-09 /pmc/articles/PMC7710148/ /pubmed/32907876 http://dx.doi.org/10.1074/mcp.TIR120.002155 Text en © 2020 Griss et al. Author's Choice—Final version open access under the terms of the Creative Commons CC-BY license (http://creativecommons.org/licenses/by/4.0) .
spellingShingle Technological Innovation and Resources
Griss, Johannes
Viteri, Guilherme
Sidiropoulos, Konstantinos
Nguyen, Vy
Fabregat, Antonio
Hermjakob, Henning
ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis
title ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis
title_full ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis
title_fullStr ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis
title_full_unstemmed ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis
title_short ReactomeGSA - Efficient Multi-Omics Comparative Pathway Analysis
title_sort reactomegsa - efficient multi-omics comparative pathway analysis
topic Technological Innovation and Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710148/
https://www.ncbi.nlm.nih.gov/pubmed/32907876
http://dx.doi.org/10.1074/mcp.TIR120.002155
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