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TIMER2.0 for analysis of tumor-infiltrating immune cells

Tumor progression and the efficacy of immunotherapy are strongly influenced by the composition and abundance of immune cells in the tumor microenvironment. Due to the limitations of direct measurement methods, computational algorithms are often used to infer immune cell composition from bulk tumor t...

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Detalles Bibliográficos
Autores principales: Li, Taiwen, Fu, Jingxin, Zeng, Zexian, Cohen, David, Li, Jing, Chen, Qianming, Li, Bo, Liu, X Shirley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319575/
https://www.ncbi.nlm.nih.gov/pubmed/32442275
http://dx.doi.org/10.1093/nar/gkaa407
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author Li, Taiwen
Fu, Jingxin
Zeng, Zexian
Cohen, David
Li, Jing
Chen, Qianming
Li, Bo
Liu, X Shirley
author_facet Li, Taiwen
Fu, Jingxin
Zeng, Zexian
Cohen, David
Li, Jing
Chen, Qianming
Li, Bo
Liu, X Shirley
author_sort Li, Taiwen
collection PubMed
description Tumor progression and the efficacy of immunotherapy are strongly influenced by the composition and abundance of immune cells in the tumor microenvironment. Due to the limitations of direct measurement methods, computational algorithms are often used to infer immune cell composition from bulk tumor transcriptome profiles. These estimated tumor immune infiltrate populations have been associated with genomic and transcriptomic changes in the tumors, providing insight into tumor–immune interactions. However, such investigations on large-scale public data remain challenging. To lower the barriers for the analysis of complex tumor–immune interactions, we significantly improved our previous web platform TIMER. Instead of just using one algorithm, TIMER2.0 (http://timer.cistrome.org/) provides more robust estimation of immune infiltration levels for The Cancer Genome Atlas (TCGA) or user-provided tumor profiles using six state-of-the-art algorithms. TIMER2.0 provides four modules for investigating the associations between immune infiltrates and genetic or clinical features, and four modules for exploring cancer-related associations in the TCGA cohorts. Each module can generate a functional heatmap table, enabling the user to easily identify significant associations in multiple cancer types simultaneously. Overall, the TIMER2.0 web server provides comprehensive analysis and visualization functions of tumor infiltrating immune cells.
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spelling pubmed-73195752020-07-01 TIMER2.0 for analysis of tumor-infiltrating immune cells Li, Taiwen Fu, Jingxin Zeng, Zexian Cohen, David Li, Jing Chen, Qianming Li, Bo Liu, X Shirley Nucleic Acids Res Web Server Issue Tumor progression and the efficacy of immunotherapy are strongly influenced by the composition and abundance of immune cells in the tumor microenvironment. Due to the limitations of direct measurement methods, computational algorithms are often used to infer immune cell composition from bulk tumor transcriptome profiles. These estimated tumor immune infiltrate populations have been associated with genomic and transcriptomic changes in the tumors, providing insight into tumor–immune interactions. However, such investigations on large-scale public data remain challenging. To lower the barriers for the analysis of complex tumor–immune interactions, we significantly improved our previous web platform TIMER. Instead of just using one algorithm, TIMER2.0 (http://timer.cistrome.org/) provides more robust estimation of immune infiltration levels for The Cancer Genome Atlas (TCGA) or user-provided tumor profiles using six state-of-the-art algorithms. TIMER2.0 provides four modules for investigating the associations between immune infiltrates and genetic or clinical features, and four modules for exploring cancer-related associations in the TCGA cohorts. Each module can generate a functional heatmap table, enabling the user to easily identify significant associations in multiple cancer types simultaneously. Overall, the TIMER2.0 web server provides comprehensive analysis and visualization functions of tumor infiltrating immune cells. Oxford University Press 2020-07-02 2020-05-22 /pmc/articles/PMC7319575/ /pubmed/32442275 http://dx.doi.org/10.1093/nar/gkaa407 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Web Server Issue
Li, Taiwen
Fu, Jingxin
Zeng, Zexian
Cohen, David
Li, Jing
Chen, Qianming
Li, Bo
Liu, X Shirley
TIMER2.0 for analysis of tumor-infiltrating immune cells
title TIMER2.0 for analysis of tumor-infiltrating immune cells
title_full TIMER2.0 for analysis of tumor-infiltrating immune cells
title_fullStr TIMER2.0 for analysis of tumor-infiltrating immune cells
title_full_unstemmed TIMER2.0 for analysis of tumor-infiltrating immune cells
title_short TIMER2.0 for analysis of tumor-infiltrating immune cells
title_sort timer2.0 for analysis of tumor-infiltrating immune cells
topic Web Server Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319575/
https://www.ncbi.nlm.nih.gov/pubmed/32442275
http://dx.doi.org/10.1093/nar/gkaa407
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