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Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data
Mapping cell types across a tissue is a central concern of spatial biology, but cell type abundance is difficult to extract from spatial gene expression data. We introduce SpatialDecon, an algorithm for quantifying cell populations defined by single cell sequencing within the regions of spatial gene...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770643/ https://www.ncbi.nlm.nih.gov/pubmed/35046414 http://dx.doi.org/10.1038/s41467-022-28020-5 |
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author | Danaher, Patrick Kim, Youngmi Nelson, Brenn Griswold, Maddy Yang, Zhi Piazza, Erin Beechem, Joseph M. |
author_facet | Danaher, Patrick Kim, Youngmi Nelson, Brenn Griswold, Maddy Yang, Zhi Piazza, Erin Beechem, Joseph M. |
author_sort | Danaher, Patrick |
collection | PubMed |
description | Mapping cell types across a tissue is a central concern of spatial biology, but cell type abundance is difficult to extract from spatial gene expression data. We introduce SpatialDecon, an algorithm for quantifying cell populations defined by single cell sequencing within the regions of spatial gene expression studies. SpatialDecon incorporates several advancements in gene expression deconvolution. We propose an algorithm harnessing log-normal regression and modelling background, outperforming classical least-squares methods. We compile cell profile matrices for 75 tissue types. We identify genes whose minimal expression by cancer cells makes them suitable for immune deconvolution in tumors. Using lung tumors, we create a dataset for benchmarking deconvolution methods against marker proteins. SpatialDecon is a simple and flexible tool for mapping cell types in spatial gene expression studies. It obtains cell abundance estimates that are spatially resolved, granular, and paired with highly multiplexed gene expression data. |
format | Online Article Text |
id | pubmed-8770643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87706432022-02-04 Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data Danaher, Patrick Kim, Youngmi Nelson, Brenn Griswold, Maddy Yang, Zhi Piazza, Erin Beechem, Joseph M. Nat Commun Article Mapping cell types across a tissue is a central concern of spatial biology, but cell type abundance is difficult to extract from spatial gene expression data. We introduce SpatialDecon, an algorithm for quantifying cell populations defined by single cell sequencing within the regions of spatial gene expression studies. SpatialDecon incorporates several advancements in gene expression deconvolution. We propose an algorithm harnessing log-normal regression and modelling background, outperforming classical least-squares methods. We compile cell profile matrices for 75 tissue types. We identify genes whose minimal expression by cancer cells makes them suitable for immune deconvolution in tumors. Using lung tumors, we create a dataset for benchmarking deconvolution methods against marker proteins. SpatialDecon is a simple and flexible tool for mapping cell types in spatial gene expression studies. It obtains cell abundance estimates that are spatially resolved, granular, and paired with highly multiplexed gene expression data. Nature Publishing Group UK 2022-01-19 /pmc/articles/PMC8770643/ /pubmed/35046414 http://dx.doi.org/10.1038/s41467-022-28020-5 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 Danaher, Patrick Kim, Youngmi Nelson, Brenn Griswold, Maddy Yang, Zhi Piazza, Erin Beechem, Joseph M. Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data |
title | Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data |
title_full | Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data |
title_fullStr | Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data |
title_full_unstemmed | Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data |
title_short | Advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data |
title_sort | advances in mixed cell deconvolution enable quantification of cell types in spatial transcriptomic data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770643/ https://www.ncbi.nlm.nih.gov/pubmed/35046414 http://dx.doi.org/10.1038/s41467-022-28020-5 |
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