ArticlePLoS computational biology2026
SHADE: A multilevel Bayesian framework for modeling directional spatial interactions in tissue microenvironments.
Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Digital immune twins and ai-integrated multi-omic biomarkers: Redefining personalized immunotherapy in non-small cell lung cancer.Iranian journal of basic medical sciences · 2026Review
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Abstract
motivationUnderstanding how different cell types interact spatially within tissue microenvironments is critical for deciphering immune dynamics, tumor progression, and tissue organization. Many current spatial analysis methods assume symmetric associations or compute image-level summaries separately without sharing information across patients and cohorts, limiting biological interpretability and statistical power.
resultsWe 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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