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A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics
Spatial transcriptomics technologies are used to profile transcriptomes while preserving spatial information, which enables high-resolution characterization of transcriptional patterns and reconstruction of tissue architecture. Due to the existence of low-resolution spots in recent spatial transcrip...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027878/ https://www.ncbi.nlm.nih.gov/pubmed/36941264 http://dx.doi.org/10.1038/s41467-023-37168-7 |
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author | Li, Haoyang Zhou, Juexiao Li, Zhongxiao Chen, Siyuan Liao, Xingyu Zhang, Bin Zhang, Ruochi Wang, Yu Sun, Shiwei Gao, Xin |
author_facet | Li, Haoyang Zhou, Juexiao Li, Zhongxiao Chen, Siyuan Liao, Xingyu Zhang, Bin Zhang, Ruochi Wang, Yu Sun, Shiwei Gao, Xin |
author_sort | Li, Haoyang |
collection | PubMed |
description | Spatial transcriptomics technologies are used to profile transcriptomes while preserving spatial information, which enables high-resolution characterization of transcriptional patterns and reconstruction of tissue architecture. Due to the existence of low-resolution spots in recent spatial transcriptomics technologies, uncovering cellular heterogeneity is crucial for disentangling the spatial patterns of cell types, and many related methods have been proposed. Here, we benchmark 18 existing methods resolving a cellular deconvolution task with 50 real-world and simulated datasets by evaluating the accuracy, robustness, and usability of the methods. We compare these methods comprehensively using different metrics, resolutions, spatial transcriptomics technologies, spot numbers, and gene numbers. In terms of performance, CARD, Cell2location, and Tangram are the best methods for conducting the cellular deconvolution task. To refine our comparative results, we provide decision-tree-style guidelines and recommendations for method selection and their additional features, which will help users easily choose the best method for fulfilling their concerns. |
format | Online Article Text |
id | pubmed-10027878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100278782023-03-22 A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics Li, Haoyang Zhou, Juexiao Li, Zhongxiao Chen, Siyuan Liao, Xingyu Zhang, Bin Zhang, Ruochi Wang, Yu Sun, Shiwei Gao, Xin Nat Commun Article Spatial transcriptomics technologies are used to profile transcriptomes while preserving spatial information, which enables high-resolution characterization of transcriptional patterns and reconstruction of tissue architecture. Due to the existence of low-resolution spots in recent spatial transcriptomics technologies, uncovering cellular heterogeneity is crucial for disentangling the spatial patterns of cell types, and many related methods have been proposed. Here, we benchmark 18 existing methods resolving a cellular deconvolution task with 50 real-world and simulated datasets by evaluating the accuracy, robustness, and usability of the methods. We compare these methods comprehensively using different metrics, resolutions, spatial transcriptomics technologies, spot numbers, and gene numbers. In terms of performance, CARD, Cell2location, and Tangram are the best methods for conducting the cellular deconvolution task. To refine our comparative results, we provide decision-tree-style guidelines and recommendations for method selection and their additional features, which will help users easily choose the best method for fulfilling their concerns. Nature Publishing Group UK 2023-03-21 /pmc/articles/PMC10027878/ /pubmed/36941264 http://dx.doi.org/10.1038/s41467-023-37168-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Haoyang Zhou, Juexiao Li, Zhongxiao Chen, Siyuan Liao, Xingyu Zhang, Bin Zhang, Ruochi Wang, Yu Sun, Shiwei Gao, Xin A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics |
title | A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics |
title_full | A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics |
title_fullStr | A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics |
title_full_unstemmed | A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics |
title_short | A comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics |
title_sort | comprehensive benchmarking with practical guidelines for cellular deconvolution of spatial transcriptomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027878/ https://www.ncbi.nlm.nih.gov/pubmed/36941264 http://dx.doi.org/10.1038/s41467-023-37168-7 |
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