HisToSpatialCNV: an interpretable deep learning method predicting spatial copy number variations from histopathology images

Copy number variations (CNV) are key drivers of cancer progression, yet methods for predicting spatial CNVs directly from haematoxylin and eosin (H&E) images are currently lacking. We introduce HisToSpatialCNV, a multiscale deep-learning framework that integrates histopathological features from H&E-stained images to infer spatial CNV patterns. Combining interpretable feature extraction with graph neural networks and multihead self-attention, our approach captures both local and global tissue contexts. Applied to HER2+ breast cancer, skin cancer and brain cancer datasets, HisToSpatialCNV outperformed existing methods for spatial gene expression inference and showed strong concordance between predicted CNVs and gene expression. In addition, it enabled tumour subclone identification, phylogenetic reconstruction and detection of pathway alterations linked to tumour progression. HisToSpatialCNV generalized across Visium and Xenium spatial transcriptomics platforms, on HER2+ patients. Applying the HisToSpatialCNV HER2+ model to TCGA HER2+ histopathology data identified spatial-molecular subtypes associated with distinct survival outcomes in TCGA HER2+ patients. By connecting histopathology to spatial genomics, HisToSpatialCNV offers a powerful, cost-effective tool for studying intratumour heterogeneity using only routine pathology images.

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Publication Details

Journal
Nature Biomedical Engineering
Published
2026-08-24
DOI
https://doi.org/10.1038/s41551-026-01754-z
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

HisToSpatialCNV: an interpretable deep learning method predicting spatial copy number variations from histopathology images

Tianao Chen, Xuhui Guo, Jing Zheng, Weiping Zou et al.
Nature Biomedical Engineering
Single-cell and spatial transcriptomics
article

HisToSpatialCNV: an interpretable deep learning method predicting spatial copy number variations from histopathology images

Tianao Chen, Xuhui Guo, Jing Zheng, Weiping Zou, Thatchayut Unjitwattana, Lana X. Garmire, Shu Zhou, Pooja Thakur, Yuheng Du, Yiwen Yang
article en

Abstract

Copy number variations (CNV) are key drivers of cancer progression, yet methods for predicting spatial CNVs directly from haematoxylin and eosin (H&E) images are currently lacking. We introduce HisToSpatialCNV, a multiscale deep-learning framework that integrates histopathological features from H&E-stained images to infer spatial CNV patterns. Combining interpretable feature extraction with graph neural networks and multihead self-attention, our approach captures both local and global tissue contexts. Applied to HER2+ breast cancer, skin cancer and brain cancer datasets, HisToSpatialCNV outperformed existing methods for spatial gene expression inference and showed strong concordance between predicted CNVs and gene expression. In addition, it enabled tumour subclone identification, phylogenetic reconstruction and detection of pathway alterations linked to tumour progression. HisToSpatialCNV generalized across Visium and Xenium spatial transcriptomics platforms, on HER2+ patients. Applying the HisToSpatialCNV HER2+ model to TCGA HER2+ histopathology data identified spatial-molecular subtypes associated with distinct survival outcomes in TCGA HER2+ patients. By connecting histopathology to spatial genomics, HisToSpatialCNV offers a powerful, cost-effective tool for studying intratumour heterogeneity using only routine pathology images.

Nature Biomedical Engineering
University of Michigan (US), University of Alabama at Birmingham (US), Parker Institute for Cancer Immunotherapy (US)
Yale University, National Institutes of Health, NIH Office of the Director, U.S. National Library of Medicine
Openalex Percentile: Top 17%
Single-cell and spatial transcriptomics
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