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Updated: Feb 4, 2026

Mining Spatial Transcriptomics Datasets using DeepSpaceDB
Published on: September 5, 2025
PathCLAST: pathway-augmented contrastive learning with attention for interpretable spatial transcriptomics
Minho Noh1, Sungkyung Lee1, Sunghyun Kim2
1Department of Computer Science and Artificial Intelligence, Dongguk University, 30, Pildong-ro 1-gil, Jung-gu, Seoul 04620, South Korea.
Abstract:
Deciphering how molecular programs are spatially organized within tissues is pivotal for understanding tumor evolution and microenvironmental interactions. Existing spatial transcriptomics tools either rely on gene-level features, ignoring the rich topology of biological pathways, or deliver black-box clusters with little mechanistic insight; thus, they limit their translational impact. A method that simultaneously leverages pathway structures and spatially matched histopathology could produce domain delineations that are both accurate and biologically interpretable. We introduce PathCLAST (Pathway-augmented Contrastive Learning with Attention for interpretable Spatial Transcriptomics), which is a framework that integrates gene expression, histopathological images, and curated pathway graphs via bi-modal contrastive learning. By embedding expression profiles into biologically structured graphs, and aligning them with local image features, PathCLAST achieves state-of-the-art spatial domain identification on multiple public datasets, while offering pathway-level attention scores for mechanistic interpretation. The pathway embedding also serves as an explicit, biology-informed dimensionality reduction scheme. PathCLAST not only uncovers domain-specific pathways and spatially organized signaling activities, but also quantifies intra-domain heterogeneity, spatial autocorrelation, and inter-domain crosstalk, providing fine-grained insights into tumor progression and tissue architecture. PathCLAST is available at https://github.com/sslim-aidrug/PathCLAST.
Insights
PathCLAST integrates gene expression, histopathology, and pathway data for advanced spatial transcriptomics. This novel framework enhances tumor microenvironment analysis and biological interpretation.
Area of Science:
- Computational Biology
- Genomics
- Bioinformatics
Background:
- Understanding molecular programs in tissues is crucial for tumor evolution and microenvironment studies.
- Current spatial transcriptomics methods lack biological interpretability and pathway topology integration.
Purpose of the Study:
- To develop a novel framework for interpretable spatial transcriptomics analysis.
- To integrate gene expression, histopathology, and pathway structures for accurate domain identification.
Main Methods:
- Introduced PathCLAST (Pathway-augmented Contrastive Learning with Attention for interpretable Spatial Transcriptomics).
- Utilized bi-modal contrastive learning to integrate gene expression, histopathology images, and pathway graphs.
- Employed pathway embedding for biology-informed dimensionality reduction.
Main Results:
- Achieved state-of-the-art spatial domain identification on multiple public datasets.
- Provided pathway-level attention scores for mechanistic interpretation.
- Uncovered domain-specific pathways, signaling activities, intra-domain heterogeneity, and inter-domain crosstalk.
Conclusions:
- PathCLAST offers accurate and biologically interpretable spatial domain delineation.
- The framework provides fine-grained insights into tumor progression and tissue architecture.
- PathCLAST enhances translational impact in cancer research and spatial biology.
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