HierarchicalDAEW achieves the strongest correlation with ground-truth expression, with gains that hold up under multi-seed reproducibility checks and negative controls that rule out positional shortcuts.
Abstract
Spatial transcriptomics assays remain costly and technically demanding, restricting transcriptome-wide profiling to specialist settings and preventing routine clinical deployment. Predicting spatially resolved gene expression from H&E histology could close this gap, yet current methods largely ignore the underlying tissue architecture and rarely quantify how their predictions can be trusted. We introduce HierarchicalDAEW, a dual-graph architecture that addresses both gaps. On the spot graph, a Domain-Aware Edge-Weighted convolutional operator learns separate projections for inter-domain, intra-domain, and boundary edges derived from Leiden clustering, allowing the model to treat tissue heterogeneity as an explicit structural signal rather than an implicit one. A second gene-level graph then fuses protein-protein interaction priors from STRING-DB with tissue-specific co-expression through learned attention gating, propagating predictions from a landmark gene set to a broader gene panel. Reliability is handled through evidential uncertainty estimation, which produces far better calibrated confidence intervals than Monte Carlo dropout under identical conditions. Across six human Visium sections spanning breast, colorectal, prostate, and cerebellar tissue, and against thirteen published baselines, HierarchicalDAEW achieves the strongest correlation with ground-truth expression, with gains that hold up under multi-seed reproducibility checks and negative controls that rule out positional shortcuts. Ablations further confirm that both the domain-aware edge typing and the hierarchical depth are necessary to this improvement, and calibrated uncertainty estimates identify low-confidence predictions for pathologist review before clinical action.
A systematic ablation study providing evidence-based design guidance for spatial transcriptomics GNNs is provided, with findings support using GAT attention and contrastive learning and investing in node feature quality over edge feature complexity.
M. Al-Taie, Firas Hazzaa, Akram Qashou et al.· BMC Bioinformatics· 0 citations
Spatial transcriptomics (ST) enables the simultaneous measurement of high-throughput gene expression and spatial structural information, offering a powerful means to decipher tissue heterogeneity. However, current spatial domain identification methods struggle to accurately distinguish continuous biological boundaries,...
Jiazhou Chen, Ziru Xiao, Junyu Li et al.· Proceedings of the 32nd ACM...· 0 citations
GatorTrio is proposed, a topology-refined tri-view graph learning framework that adaptively fuses views per unit via an interaction-aware sparse Mixture-of-Experts (MoE) router and refine topology through self-training by pruning pseudo-label–inconsistent inter-cluster edges and re-encoding on the refined graphs.
Zhenhao Zhang, Jun Shen, Jiang Bian et al.· Proceedings of the 32nd ACM...· 0 citations
MultiSpaceNet is presented, a graph-based framework for joint representation learning from paired spatial transcriptomic and proteomic data that outperforms nine published state-of-the-art methods in spatial domain identification and preserves biological structure across replicate sections better than all compared alte...
Zheng-Qiang Zhang, Bing-Hong Chen, Jing-Yi Bai et al.· Bioinformatics· 0 citations
Abstract Paired spatial multi-omics provides a supervised basis for learning RNA–protein correspondence in situ, but predicting protein abundance from spatial transcriptomic data alone remains challenging across tissue contexts and protein panels. Here, we present DPAS-Graph, an adaptive relation-learning framework for...
Spatial transcriptomics (ST) profiles gene expression within tissue architecture, but its cost and experimental complexity limit routine use. Predicting spatial expression from routinely available hematoxylin and eosin (HE) images therefore offers a scalable alternative. However, conventional methods often fit high-dim...
Shi-Ting Ruan, Xi-Tong Ling, Qi-Ming He et al.· 0 citations
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