A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomics

A major challenge in spatial transcriptomics (ST) is resolving cellular composition, especially in technologies lacking single-cell resolution. The mixture of transcriptional signals within spatial spots complicates deconvolution and downstream analyses. To uncover the spatial heterogeneity of tissu...

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Main Authors: Xuan Li, Yincai Tang, Jingsi Ming, Xingjie Shi
Format: Article
Language:English
Published: Taylor & Francis Group 2025-04-01
Series:Statistical Theory and Related Fields
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Online Access:https://www.tandfonline.com/doi/10.1080/24754269.2025.2495651
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author Xuan Li
Yincai Tang
Jingsi Ming
Xingjie Shi
author_facet Xuan Li
Yincai Tang
Jingsi Ming
Xingjie Shi
author_sort Xuan Li
collection DOAJ
description A major challenge in spatial transcriptomics (ST) is resolving cellular composition, especially in technologies lacking single-cell resolution. The mixture of transcriptional signals within spatial spots complicates deconvolution and downstream analyses. To uncover the spatial heterogeneity of tissues, we introduce SvdRFCTD, a reference-free spatial transcriptomics deconvolution method, which estimates the cell type proportions at each spot on the tissue. To fully capture the heterogeneity in the ST data, we combine SvdRFCTD with a Bayesian hierarchical negative binomial model with spatial effects incorporated in both the mean and dispersion of the gene expression, which is used to explicitly model the generative mechanism of cell type proportions. By integrating spatial information and leveraging marker gene information, SvdRFCTD accurately estimates cell type proportions and uncovers complex spatial patterns. We demonstrate the ability of SvdRFCTD to identify cell types on simulated datasets. By applying SvdRFCTD to mouse brain and human pancreatic ductal adenocarcinomas datasets, we observe significant cellular heterogeneity within the tissue sections and successfully identify regions with high proportions of aggregated cell types, along with the spatial relationships between different cell types.
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spelling doaj-art-6a7ea85720e84b69a8d5230f2363dbf72025-08-20T03:13:30ZengTaylor & Francis GroupStatistical Theory and Related Fields2475-42692475-42772025-04-019217821210.1080/24754269.2025.2495651A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomicsXuan Li0Yincai Tang1Jingsi Ming2Xingjie Shi3KLATASDS-MOE, School of Statistics, East China Normal University, Shanghai, People's Republic of ChinaKLATASDS-MOE, School of Statistics, East China Normal University, Shanghai, People's Republic of ChinaKLATASDS-MOE, School of Statistics, East China Normal University, Shanghai, People's Republic of ChinaKLATASDS-MOE, School of Statistics, East China Normal University, Shanghai, People's Republic of ChinaA major challenge in spatial transcriptomics (ST) is resolving cellular composition, especially in technologies lacking single-cell resolution. The mixture of transcriptional signals within spatial spots complicates deconvolution and downstream analyses. To uncover the spatial heterogeneity of tissues, we introduce SvdRFCTD, a reference-free spatial transcriptomics deconvolution method, which estimates the cell type proportions at each spot on the tissue. To fully capture the heterogeneity in the ST data, we combine SvdRFCTD with a Bayesian hierarchical negative binomial model with spatial effects incorporated in both the mean and dispersion of the gene expression, which is used to explicitly model the generative mechanism of cell type proportions. By integrating spatial information and leveraging marker gene information, SvdRFCTD accurately estimates cell type proportions and uncovers complex spatial patterns. We demonstrate the ability of SvdRFCTD to identify cell types on simulated datasets. By applying SvdRFCTD to mouse brain and human pancreatic ductal adenocarcinomas datasets, we observe significant cellular heterogeneity within the tissue sections and successfully identify regions with high proportions of aggregated cell types, along with the spatial relationships between different cell types.https://www.tandfonline.com/doi/10.1080/24754269.2025.2495651Spatial transcriptomicsreference-free deconvolutiontissue heterogeneityspatial patternBayesian hierarchical model
spellingShingle Xuan Li
Yincai Tang
Jingsi Ming
Xingjie Shi
A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomics
Statistical Theory and Related Fields
Spatial transcriptomics
reference-free deconvolution
tissue heterogeneity
spatial pattern
Bayesian hierarchical model
title A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomics
title_full A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomics
title_fullStr A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomics
title_full_unstemmed A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomics
title_short A Bayesian hierarchical model with spatially varying dispersion for reference-free cell type deconvolution in spatial transcriptomics
title_sort bayesian hierarchical model with spatially varying dispersion for reference free cell type deconvolution in spatial transcriptomics
topic Spatial transcriptomics
reference-free deconvolution
tissue heterogeneity
spatial pattern
Bayesian hierarchical model
url https://www.tandfonline.com/doi/10.1080/24754269.2025.2495651
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