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Joint cell segmentation and cell type annotation for spatial transcriptomics

RNA hybridization‐based spatial transcriptomics provides unparalleled detection sensitivity. However, inaccuracies in segmentation of image volumes into cells cause misassignment of mRNAs which is a major source of errors. Here, we develop JSTA, a computational framework for joint cell segmentation...

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Autores principales: Littman, Russell, Hemminger, Zachary, Foreman, Robert, Arneson, Douglas, Zhang, Guanglin, Gómez‐Pinilla, Fernando, Yang, Xia, Wollman, Roy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166214/
https://www.ncbi.nlm.nih.gov/pubmed/34057817
http://dx.doi.org/10.15252/msb.202010108
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author Littman, Russell
Hemminger, Zachary
Foreman, Robert
Arneson, Douglas
Zhang, Guanglin
Gómez‐Pinilla, Fernando
Yang, Xia
Wollman, Roy
author_facet Littman, Russell
Hemminger, Zachary
Foreman, Robert
Arneson, Douglas
Zhang, Guanglin
Gómez‐Pinilla, Fernando
Yang, Xia
Wollman, Roy
author_sort Littman, Russell
collection PubMed
description RNA hybridization‐based spatial transcriptomics provides unparalleled detection sensitivity. However, inaccuracies in segmentation of image volumes into cells cause misassignment of mRNAs which is a major source of errors. Here, we develop JSTA, a computational framework for joint cell segmentation and cell type annotation that utilizes prior knowledge of cell type‐specific gene expression. Simulation results show that leveraging existing cell type taxonomy increases RNA assignment accuracy by more than 45%. Using JSTA, we were able to classify cells in the mouse hippocampus into 133 (sub)types revealing the spatial organization of CA1, CA3, and Sst neuron subtypes. Analysis of within cell subtype spatial differential gene expression of 80 candidate genes identified 63 with statistically significant spatial differential gene expression across 61 (sub)types. Overall, our work demonstrates that known cell type expression patterns can be leveraged to improve the accuracy of RNA hybridization‐based spatial transcriptomics while providing highly granular cell (sub)type information. The large number of newly discovered spatial gene expression patterns substantiates the need for accurate spatial transcriptomic measurements that can provide information beyond cell (sub)type labels.
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spelling pubmed-81662142021-06-16 Joint cell segmentation and cell type annotation for spatial transcriptomics Littman, Russell Hemminger, Zachary Foreman, Robert Arneson, Douglas Zhang, Guanglin Gómez‐Pinilla, Fernando Yang, Xia Wollman, Roy Mol Syst Biol Articles RNA hybridization‐based spatial transcriptomics provides unparalleled detection sensitivity. However, inaccuracies in segmentation of image volumes into cells cause misassignment of mRNAs which is a major source of errors. Here, we develop JSTA, a computational framework for joint cell segmentation and cell type annotation that utilizes prior knowledge of cell type‐specific gene expression. Simulation results show that leveraging existing cell type taxonomy increases RNA assignment accuracy by more than 45%. Using JSTA, we were able to classify cells in the mouse hippocampus into 133 (sub)types revealing the spatial organization of CA1, CA3, and Sst neuron subtypes. Analysis of within cell subtype spatial differential gene expression of 80 candidate genes identified 63 with statistically significant spatial differential gene expression across 61 (sub)types. Overall, our work demonstrates that known cell type expression patterns can be leveraged to improve the accuracy of RNA hybridization‐based spatial transcriptomics while providing highly granular cell (sub)type information. The large number of newly discovered spatial gene expression patterns substantiates the need for accurate spatial transcriptomic measurements that can provide information beyond cell (sub)type labels. John Wiley and Sons Inc. 2021-05-31 /pmc/articles/PMC8166214/ /pubmed/34057817 http://dx.doi.org/10.15252/msb.202010108 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Littman, Russell
Hemminger, Zachary
Foreman, Robert
Arneson, Douglas
Zhang, Guanglin
Gómez‐Pinilla, Fernando
Yang, Xia
Wollman, Roy
Joint cell segmentation and cell type annotation for spatial transcriptomics
title Joint cell segmentation and cell type annotation for spatial transcriptomics
title_full Joint cell segmentation and cell type annotation for spatial transcriptomics
title_fullStr Joint cell segmentation and cell type annotation for spatial transcriptomics
title_full_unstemmed Joint cell segmentation and cell type annotation for spatial transcriptomics
title_short Joint cell segmentation and cell type annotation for spatial transcriptomics
title_sort joint cell segmentation and cell type annotation for spatial transcriptomics
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166214/
https://www.ncbi.nlm.nih.gov/pubmed/34057817
http://dx.doi.org/10.15252/msb.202010108
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