bioRxivGenomicsPreprint
BRIDGE: A Multi-organ Histo-ST Foundation Model Enables Virtual Spatial Transcriptomics for Enhanced Few-shot Cancer Diagnosis
Zhuo Liang, Weiqin Zhao, Fuying WangiD, Guangyong CheniD, Yuanhua HuangiD, Lequan YuiD
Abstract
Recent studies have explored generating virtual spatial transcriptomics (ST) profiles from histological images, offering a promising alternative to laboratory-measured molecular profiling. However, existing approaches predominantly rely on single-organ models and require sub-stantial organ-specific training data, restricting their accuracy under challenging few-shot conditions in clincical practice, where less than 10 slides are available for specific organs or techniques. Here, we present BRIDGE, a multi-organ foundation model pre-trained on over 600,000 paired histology-ST profiles across 13 human organs and three sequencing techniques. By robustly aligning morphological features and genomic information within a shared multi-organ latent space, BRIDGE can leverage common biological knowledge across distinct tissues to enable accurate and generalizable pan-cancer molecular profiling. Without additional organ-specific fine-tuning, BRIDGE accurately predicts the spatial expression of 80 biomarker genes, achieving an average Pearson correlation coefficient (PCC) of 0.474--a 30% improvement over existing state-of-the-art models under three clinically challenging few-shot scenarios. With generated virtual ST, BRIDGE outperforms current state-of-the-art pathology foundation models in predicting cancer survival, achieving an average concordance index (C-index) of 0.724 across six TCGA cohorts. Notably, BRIDGE maintains exceptional performance even in zero-shot scenarios involving three cancer types not seen during its training, achieving an average C-index of 0.717, thereby demonstrating its strong generalization capability that transcends organ- and subtype-specific boundaries. Moreover, BRIDGE-generated virtual spatial transcriptomes match the prognostic accuracy of bulk RNA-seq, highlighting their potential as a spatially informative alternative to laboratory sequencing. In general, BRIDGE represents a data-efficient tool in virtual ST that facilitates biomedical discoveries in clinical few-shot contexts and advances diagnosis of understudied cancers without sufficient samples.
- organism: human
- assay: spatial transcriptomics
- assay: imaging
- research focus: drug response / drug discovery
- research focus: benchmarking
- research focus: database / resource
- research focus: software / tool
- approach: deep learning
- approach: experimental assay
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Virtual spatial transcriptomics from histopathology enables prognostic and therapeutic response prediction in cancer
Shaoqing Jiao, Zhen Yuan, … Jiajie Peng·bioRxiv·Aug 9, 2026
- STPath: A Generative Foundation Model for Integrating Spatial Transcriptomics and Whole Slide Images
Tinglin Huang, Tianyu Liu, … Wengong Jin·npj Digital MedicinePeer-reviewed·Nov 14, 2025
- H2O: A Foundation Model Bridging Histopathology to Spatial Multi-Omics Profiling
Yunjie Gu, Zihan Wu, … Jianhua Yao·bioRxiv·Apr 24, 2026
- A multimodal foundation model to integrate histology with spatial molecular programs
Zongxu Zhang, Bowen Qin, … Zexian Zeng·bioRxiv·Oct 13, 2026
- SciCore-Omics: a tri-modal foundation model unifying histology, spatial transcriptomics and language for spatial biology
Xinyu Xiao, Yunfei Li, … Fuchu He·bioRxiv·Jun 4, 2026
- Pan-cancer virtual spatial transcriptomics from routine histology with Phoenix
Manuel Tran, Rushin H. Gindra, … Tingying Peng·bioRxiv·May 7, 2026