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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Biochemistry and Molecular Biology
2020
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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. |
format | Online Article Text |
id | pubmed-7710148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
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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