A visual–omics foundation model to bridge histopathology with spatial transcriptomics

Artificial intelligence has revolutionized computational biology. Recent developments in omics technologies, including single-cell RNA sequencing and spatial transcriptomics, provide detailed genomic data alongside tissue histology. However, current computational models focus on either omics or image analysis, lacking their integration. To address this, we developed OmiCLIP, a visual-omics foundation model linking hematoxylin and eosin images and transcriptomics using tissue patches from Visium data. We transformed transcriptomic data into 'sentences' by concatenating top-expressed gene symbols from each patch. We curated a dataset of 2.2 million paired tissue images and transcriptomic data across 32 organs to train OmiCLIP integrating histology and transcriptomics. Building on OmiCLIP, our Loki platform offers five key functions: tissue alignment, annotation via bulk RNA sequencing or marker genes, cell-type decomposition, image-transcriptomics retrieval and spatial transcriptomics gene expression prediction from hematoxylin and eosin-stained images. Compared with 22 state-of-the-art models on 5 simulations, and 19 public and 4 in-house experimental datasets, Loki demonstrated consistent accuracy and robustness.

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Publication Details

Journal
Nature Methods
Published
2025-05-29
DOI
https://doi.org/10.1038/s41592-025-02707-1
Citations
45
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
36.27

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article

A visual–omics foundation model to bridge histopathology with spatial transcriptomics

Keith A. Youker, Qin Ma, Shu‐Hsia Chen, Yang Yu et al.
45 citations
Nature Methods
Single-cell and spatial transcriptomics
36.27
article

A visual–omics foundation model to bridge histopathology with spatial transcriptomics

Keith A. Youker, Qin Ma, Shu‐Hsia Chen, Yang Yu, John P. Cooke, Kristopher W. Brannan, Jun‐ichi Abe, Longhou Fang, Hao Cheng, Weiqing Chen, Pengzhi Zhang, Vrutant Shah, Li Lai, Ken Chen, Guangyu Wang, Shengyu Li, Qianqian Song, Tu Tran, Nhat‐Tu Le, Yiwei Xiao
article en
45 citations

Abstract

Artificial intelligence has revolutionized computational biology. Recent developments in omics technologies, including single-cell RNA sequencing and spatial transcriptomics, provide detailed genomic data alongside tissue histology. However, current computational models focus on either omics or image analysis, lacking their integration. To address this, we developed OmiCLIP, a visual-omics foundation model linking hematoxylin and eosin images and transcriptomics using tissue patches from Visium data. We transformed transcriptomic data into 'sentences' by concatenating top-expressed gene symbols from each patch. We curated a dataset of 2.2 million paired tissue images and transcriptomic data across 32 organs to train OmiCLIP integrating histology and transcriptomics. Building on OmiCLIP, our Loki platform offers five key functions: tissue alignment, annotation via bulk RNA sequencing or marker genes, cell-type decomposition, image-transcriptomics retrieval and spatial transcriptomics gene expression prediction from hematoxylin and eosin-stained images. Compared with 22 state-of-the-art models on 5 simulations, and 19 public and 4 in-house experimental datasets, Loki demonstrated consistent accuracy and robustness.

Nature MethodsVol. 22(7)
Houston Methodist (US), The University of Texas MD Anderson Cancer Center (US), Cornell University (US), University of Florida (US), The Ohio State University (US)
Cancer Prevention and Research Institute of Texas, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 0%
Single-cell and spatial transcriptomics
36.27
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