ArticleBriefings in bioinformatics2026
GATCL: graph attention network meets contrastive learning for spatial domain identification.
Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed.
- Multi-task spatial distillation reveals cell-type-resolved programmed cell death landscapes in the human kidney.Briefings in bioinformatics · 2026Article
- AGCLD: an adaptive graph contrastive learning method with denoising for spatial domain identification.Briefings in bioinformatics · 2026Article
- Cell type-specific dissection of cell death programs during ovarian aging.Briefings in bioinformatics · 2026Article
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5 authors.
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Abstract
Spatial domain identification is an essential task for revealing spatial heterogeneity within tissues, providing insights into disease mechanisms, tissue development, and the cellular microenvironment. In recent years, spatial multi-omics has emerged as the new frontier in spatial domain identification that offers deeper insights into the complex interplay and functional dynamics of heterogeneous cell communities within their native tissue context. Most existing methods rely on static graph structures that treat all neighboring cells uniformly, failing to capture the nuanced cellular interactions within the microenvironment and thus blurring functional boundaries. Furthermore, cross-modal reconstruction performance is often degraded by overfitting to modality-specific noise, which may impair the precise delineation of spatial domains. Therefore, we present GATCL, a novel deep learning framework that integrates a graph attention network with contrastive learning (CL) for robust spatial domain identification. First, GATCL leverages the graph attention mechanism to dynamically assign weights to neighboring spots, adaptively modeling the complex cellular architecture. Second, it implements a cross-modal CL strategy that forces representations from the same spatial location to be similar while pushing those from different locations apart, thereby achieving robust alignment between modalities. Comprehensive experiments across six distinct datasets (spanning transcriptome, proteome, and chromatin) reveal that GATCL is superior to seven representative methods across six key evaluation metrics.
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