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Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding

Spatially resolved transcriptomics provides the opportunity to investigate the gene expression profiles and the spatial context of cells in naive state, but at low transcript detection sensitivity or with limited gene throughput. Comprehensive annotating of cell types in spatially resolved transcrip...

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Autores principales: Shen, Rongbo, Liu, Lin, Wu, Zihan, Zhang, Ying, Yuan, Zhiyuan, Guo, Junfu, Yang, Fan, Zhang, Chao, Chen, Bichao, Feng, Wanwan, Liu, Chao, Guo, Jing, Fan, Guozhen, Zhang, Yong, Li, Yuxiang, Xu, Xun, Yao, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741613/
https://www.ncbi.nlm.nih.gov/pubmed/36496406
http://dx.doi.org/10.1038/s41467-022-35288-0
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author Shen, Rongbo
Liu, Lin
Wu, Zihan
Zhang, Ying
Yuan, Zhiyuan
Guo, Junfu
Yang, Fan
Zhang, Chao
Chen, Bichao
Feng, Wanwan
Liu, Chao
Guo, Jing
Fan, Guozhen
Zhang, Yong
Li, Yuxiang
Xu, Xun
Yao, Jianhua
author_facet Shen, Rongbo
Liu, Lin
Wu, Zihan
Zhang, Ying
Yuan, Zhiyuan
Guo, Junfu
Yang, Fan
Zhang, Chao
Chen, Bichao
Feng, Wanwan
Liu, Chao
Guo, Jing
Fan, Guozhen
Zhang, Yong
Li, Yuxiang
Xu, Xun
Yao, Jianhua
author_sort Shen, Rongbo
collection PubMed
description Spatially resolved transcriptomics provides the opportunity to investigate the gene expression profiles and the spatial context of cells in naive state, but at low transcript detection sensitivity or with limited gene throughput. Comprehensive annotating of cell types in spatially resolved transcriptomics to understand biological processes at the single cell level remains challenging. Here we propose Spatial-ID, a supervision-based cell typing method, that combines the existing knowledge of reference single-cell RNA-seq data and the spatial information of spatially resolved transcriptomics data. We present a series of benchmarking analyses on publicly available spatially resolved transcriptomics datasets, that demonstrate the superiority of Spatial-ID compared with state-of-the-art methods. Besides, we apply Spatial-ID on a self-collected mouse brain hemisphere dataset measured by Stereo-seq, that shows the scalability of Spatial-ID to three-dimensional large field tissues with subcellular spatial resolution.
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spelling pubmed-97416132022-12-12 Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding Shen, Rongbo Liu, Lin Wu, Zihan Zhang, Ying Yuan, Zhiyuan Guo, Junfu Yang, Fan Zhang, Chao Chen, Bichao Feng, Wanwan Liu, Chao Guo, Jing Fan, Guozhen Zhang, Yong Li, Yuxiang Xu, Xun Yao, Jianhua Nat Commun Article Spatially resolved transcriptomics provides the opportunity to investigate the gene expression profiles and the spatial context of cells in naive state, but at low transcript detection sensitivity or with limited gene throughput. Comprehensive annotating of cell types in spatially resolved transcriptomics to understand biological processes at the single cell level remains challenging. Here we propose Spatial-ID, a supervision-based cell typing method, that combines the existing knowledge of reference single-cell RNA-seq data and the spatial information of spatially resolved transcriptomics data. We present a series of benchmarking analyses on publicly available spatially resolved transcriptomics datasets, that demonstrate the superiority of Spatial-ID compared with state-of-the-art methods. Besides, we apply Spatial-ID on a self-collected mouse brain hemisphere dataset measured by Stereo-seq, that shows the scalability of Spatial-ID to three-dimensional large field tissues with subcellular spatial resolution. Nature Publishing Group UK 2022-12-10 /pmc/articles/PMC9741613/ /pubmed/36496406 http://dx.doi.org/10.1038/s41467-022-35288-0 Text en © The Author(s) 2022 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
Shen, Rongbo
Liu, Lin
Wu, Zihan
Zhang, Ying
Yuan, Zhiyuan
Guo, Junfu
Yang, Fan
Zhang, Chao
Chen, Bichao
Feng, Wanwan
Liu, Chao
Guo, Jing
Fan, Guozhen
Zhang, Yong
Li, Yuxiang
Xu, Xun
Yao, Jianhua
Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding
title Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding
title_full Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding
title_fullStr Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding
title_full_unstemmed Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding
title_short Spatial-ID: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding
title_sort spatial-id: a cell typing method for spatially resolved transcriptomics via transfer learning and spatial embedding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741613/
https://www.ncbi.nlm.nih.gov/pubmed/36496406
http://dx.doi.org/10.1038/s41467-022-35288-0
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