Sep 2026· Proceedings of the Thirty-Fifth International Joint Conference on Artificial Intelligence· 0 citations· 32 references
TL;DR
It is demonstrated that DAHGT-CCI can more accurately reconstruct cell communication networks in complex tissue microenvironments, offering an indispensable computational tool for studying developmental processes, disease mechanisms, and potential therapeutic targets from a spatially resolved perspective.
Abstract
Spatial transcriptomics has significantly advanced tissue biology and makes it possible to study the spatial interactions of cells in the microenvironment of complex tissues. However, accurately inferring intercellular communication from these data remains challenging due to the need to effectively integrate spatial topology with high-dimensional gene expression information. To address this challenge, we propose DAHGT-CCI, a novel method for inferring intercellular communication from spatial transcriptomics data. By fusing multimodal heterogeneous features to construct a unified node representation and introducing a meta-relation-aware dynamic attention mechanism, DAHGT-CCI can adaptively learn the weights of edges in the graph, thereby achieving superior precision and fine-grained inference of intercellular interactions. We evaluated the performance of DAHGT-CCI on six different spatial transcriptomics datasets. In these benchmarks, DAHGT-CCI outperformed existing graph-based learning methods and cell-cell communication inference models in terms of accuracy, AUROC, recall, and F1 score. These results demonstrate that DAHGT-CCI can more accurately reconstruct cell communication networks in complex tissue microenvironments, offering an indispensable computational tool for studying developmental processes, disease mechanisms, and potential therapeutic targets from a spatially resolved perspective.
GRAIL-Heart is presented, a graph-attention-based framework that integrates spatial tissue topology with multi-task learning to predict context-dependent L-R interactions, reconstruct gene expression, and infer causal signalling pathways in spatial transcriptomics data.
Tumo Kgabeng, Lu-Lu Wang, H. Ngwangwa et al.· MethodsX· 0 citations
Prior-enhanced Inference for Spatial Transcriptomic Cell Type Mapping (PRISM), a novel three-stage framework integrating biological prior construction, pseudo-label generation, and multi-level ST refinement, shows strong robustness to domain shift and platform heterogeneity.
Yiheng Xu, Xuehao Wang, Shuqi Liu et al.· Bioinform.· 0 citations
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Iñigo Clemente‐Larramendi, S. Hillion, D. Cornec et al.· bioRxiv· 0 citations
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Experiments demonstrate that the GraphFusionNN fusion strategy— integrating graph topology, spatial context, and external embeddings—significantly improves classification accuracy, macro-F1, and robustness compared to single-modality models.
CoReGRN (Contextual Refinement of Gene Regulatory Networks), a nonparametric, context-aware post-processing framework that refines inferred GRNs by reweighting candidate regulatory interactions using Mutual Information based association strength and local network context, is proposed.
E. M., Jereesh A. S., G. S. Kumar· BMC Genomics· 0 citations
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