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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8166214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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