SHADE: A multilevel Bayesian framework for modeling directional spatial interactions in tissue microenvironments

We present SHADE (Spatial Hierarchical Asymmetry via Directional Estimation), a multilevel Bayesian framework for modeling asymmetric spatial interactions across scales. SHADE quantifies direction-specific cell-cell associations using smooth spatial interaction curves (SICs) and integrates data across tissue sections, patients, and cohorts. Through simulation studies, SHADE demonstrates improved accuracy, robustness, and interpretability over existing methods. Application to colorectal cancer multiplexed imaging data demonstrates SHADE's ability to quantify directional spatial patterns while controlling for tissue architecture confounders and capturing substantial patient-level heterogeneity. The framework successfully identifies biologically interpretable spatial organization patterns, revealing that local microenvironmental structure varies considerably across patients within molecular subtypes.

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Publication Details

Journal
PLoS Computational Biology
Published
2026-02-04
DOI
https://doi.org/10.1371/journal.pcbi.1013930
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

SHADE: A multilevel Bayesian framework for modeling directional spatial interactions in tissue microenvironments

Joel Eliason, Michele Peruzzi, Arvind Rao
PLoS Computational Biology
Single-cell and spatial transcriptomics
article

SHADE: A multilevel Bayesian framework for modeling directional spatial interactions in tissue microenvironments

Joel Eliason, Michele Peruzzi, Arvind Rao
article en

Abstract

We present SHADE (Spatial Hierarchical Asymmetry via Directional Estimation), a multilevel Bayesian framework for modeling asymmetric spatial interactions across scales. SHADE quantifies direction-specific cell-cell associations using smooth spatial interaction curves (SICs) and integrates data across tissue sections, patients, and cohorts. Through simulation studies, SHADE demonstrates improved accuracy, robustness, and interpretability over existing methods. Application to colorectal cancer multiplexed imaging data demonstrates SHADE's ability to quantify directional spatial patterns while controlling for tissue architecture confounders and capturing substantial patient-level heterogeneity. The framework successfully identifies biologically interpretable spatial organization patterns, revealing that local microenvironmental structure varies considerably across patients within molecular subtypes.

PLoS Computational BiologyVol. 22(2)
Johns Hopkins University (US), University of Michigan (US), Michigan United (US)
Openalex Percentile: Top 67%
Single-cell and spatial transcriptomics
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