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Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data
Recent technological advancements have enabled spatially resolved transcriptomic profiling but at multi-cellular pixel resolution, thereby hindering the identification of cell-type-specific spatial patterns and gene expression variation. To address this challenge, we develop STdeconvolve as a refere...
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/PMC9055051/ https://www.ncbi.nlm.nih.gov/pubmed/35487922 http://dx.doi.org/10.1038/s41467-022-30033-z |
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author | Miller, Brendan F. Huang, Feiyang Atta, Lyla Sahoo, Arpan Fan, Jean |
author_facet | Miller, Brendan F. Huang, Feiyang Atta, Lyla Sahoo, Arpan Fan, Jean |
author_sort | Miller, Brendan F. |
collection | PubMed |
description | Recent technological advancements have enabled spatially resolved transcriptomic profiling but at multi-cellular pixel resolution, thereby hindering the identification of cell-type-specific spatial patterns and gene expression variation. To address this challenge, we develop STdeconvolve as a reference-free approach to deconvolve underlying cell types comprising such multi-cellular pixel resolution spatial transcriptomics (ST) datasets. Using simulated as well as real ST datasets from diverse spatial transcriptomics technologies comprising a variety of spatial resolutions such as Spatial Transcriptomics, 10X Visium, DBiT-seq, and Slide-seq, we show that STdeconvolve can effectively recover cell-type transcriptional profiles and their proportional representation within pixels without reliance on external single-cell transcriptomics references. STdeconvolve provides comparable performance to existing reference-based methods when suitable single-cell references are available, as well as potentially superior performance when suitable single-cell references are not available. STdeconvolve is available as an open-source R software package with the source code available at https://github.com/JEFworks-Lab/STdeconvolve. |
format | Online Article Text |
id | pubmed-9055051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90550512022-05-01 Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data Miller, Brendan F. Huang, Feiyang Atta, Lyla Sahoo, Arpan Fan, Jean Nat Commun Article Recent technological advancements have enabled spatially resolved transcriptomic profiling but at multi-cellular pixel resolution, thereby hindering the identification of cell-type-specific spatial patterns and gene expression variation. To address this challenge, we develop STdeconvolve as a reference-free approach to deconvolve underlying cell types comprising such multi-cellular pixel resolution spatial transcriptomics (ST) datasets. Using simulated as well as real ST datasets from diverse spatial transcriptomics technologies comprising a variety of spatial resolutions such as Spatial Transcriptomics, 10X Visium, DBiT-seq, and Slide-seq, we show that STdeconvolve can effectively recover cell-type transcriptional profiles and their proportional representation within pixels without reliance on external single-cell transcriptomics references. STdeconvolve provides comparable performance to existing reference-based methods when suitable single-cell references are available, as well as potentially superior performance when suitable single-cell references are not available. STdeconvolve is available as an open-source R software package with the source code available at https://github.com/JEFworks-Lab/STdeconvolve. Nature Publishing Group UK 2022-04-29 /pmc/articles/PMC9055051/ /pubmed/35487922 http://dx.doi.org/10.1038/s41467-022-30033-z 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 Miller, Brendan F. Huang, Feiyang Atta, Lyla Sahoo, Arpan Fan, Jean Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data |
title | Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data |
title_full | Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data |
title_fullStr | Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data |
title_full_unstemmed | Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data |
title_short | Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data |
title_sort | reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055051/ https://www.ncbi.nlm.nih.gov/pubmed/35487922 http://dx.doi.org/10.1038/s41467-022-30033-z |
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