STHELAR, a multi-tissue dataset linking spatial transcriptomics and histology for cell type annotation

Understanding the composition of the tumor microenvironment is critical for cancer research. Spatial transcriptomics profiles gene expressions in spatial context, revealing tissue architecture and cellular heterogeneity, but its cost and technical complexity limit adoption. To address this issue, we introduce a pipeline to build STHELAR, a large-scale dataset that integrates spatial transcriptomics with Hematoxylin and Eosin (H&E) whole-slide images for cell type annotation. The dataset comprises 31 human Xenium FFPE sections across 16 tissue types, for 22 cancerous and 9 non-cancerous patients. It contains over 11 million unique biological cells, each assigned to one of ten curated cell-type categories designed to accommodate a pan-cancer setting. Annotations were derived through Tangram-based alignment to single-cell reference atlases, followed by slide-specific clustering and differential expression analysis. Co-registered H&E images enabled the extraction of over 500,000 patches with segmentation and classification masks. Quality control steps assessed segmentation accuracy, filtered out low-confidence regions, and verified annotation integrity. STHELAR provides a reference resource for developing models to predict cell-type annotations directly from histological images.

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Publication Details

Journal
Scientific Data
Published
2026-03-12
DOI
https://doi.org/10.1038/s41597-026-06937-6
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
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article

STHELAR, a multi-tissue dataset linking spatial transcriptomics and histology for cell type annotation

Paul-Henry Cournède, Quentin Blampey, Hakim Benkirane, Stergios Christodoulidis et al.
Scientific Data
Single-cell and spatial transcriptomics
article

STHELAR, a multi-tissue dataset linking spatial transcriptomics and histology for cell type annotation

Paul-Henry Cournède, Quentin Blampey, Hakim Benkirane, Stergios Christodoulidis, Arianna Marinello, Félicie Giraud-Sauveur
article en

Abstract

Understanding the composition of the tumor microenvironment is critical for cancer research. Spatial transcriptomics profiles gene expressions in spatial context, revealing tissue architecture and cellular heterogeneity, but its cost and technical complexity limit adoption. To address this issue, we introduce a pipeline to build STHELAR, a large-scale dataset that integrates spatial transcriptomics with Hematoxylin and Eosin (H&E) whole-slide images for cell type annotation. The dataset comprises 31 human Xenium FFPE sections across 16 tissue types, for 22 cancerous and 9 non-cancerous patients. It contains over 11 million unique biological cells, each assigned to one of ten curated cell-type categories designed to accommodate a pan-cancer setting. Annotations were derived through Tangram-based alignment to single-cell reference atlases, followed by slide-specific clustering and differential expression analysis. Co-registered H&E images enabled the extraction of over 500,000 patches with segmentation and classification masks. Quality control steps assessed segmentation accuracy, filtered out low-confidence regions, and verified annotation integrity. STHELAR provides a reference resource for developing models to predict cell-type annotations directly from histological images.

Scientific Data
Université Paris-Saclay (FR), Institut Gustave Roussy (FR), CentraleSupélec (FR)
Industry, innovation and infrastructure
Openalex Percentile: Top 25%
Single-cell and spatial transcriptomics
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