ArticlePLoS computational biology2026
Spatially guided translation from histology images to transcriptomic profiles using foundation model-driven contrastive learning.
Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Spatial transcriptomics (ST) enhances single-cell RNA sequencing by revealing transcript distribution, offering critical insights into heterogeneous diseases such as breast cancer. However, the high cost and lengthy processes of generating high-quality ST data limit clinical application. Recent deep learning methods predict ST from histology images, but often fail to capture both morphological features and spatial context. We introduce FOCST, a foundation model-driven framework for ST imputation that leverages spatial guided contrastive learning. FOCST begins with UNI, a large histopathology foundation model, to extract visual features from tissue images. These are integrated with expression data in a unified embedding space via contrastive learning, enabling cross-modal prediction and imputation. To further enhance spatial awareness, a graph neural network incorporates positional information, improving regional detection and interpretability.Benchmarking demonstrates FOCST's superior performance over state-of-the-art methods and alternative vision encoders (paired Wilcoxon signed-rank tests, FDR-adjusted p < 0.05, N = 6 images). Predicted profiles enable clinically relevant downstream analyses, including patient stratification by treatment response (ROC AUC (Receiver Operating Characteristic - Area Under the Curve) = 0.79). Our results highlight the promise of combining foundation models and spatially guided learning to efficiently generate ST insights, advancing cancer research and precision medicine.
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