ArticleBriefings in bioinformatics2026
SpatialDG: a novel spatial domain identification method for spatially resolved transcriptomics data based on dual-graph neural network.
Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Spatially resolved transcriptomic (ST) technologies offer transformative opportunities to chart gene expression landscapes within intact tissue architecture. Uncovering spatially discrete domains of biological function is essential for deciphering tissue heterogeneity, developmental processes, and disease mechanisms. Yet, the inherent noise, high dimensionality, and spatial sparsity of ST data present substantial challenges to the unsupervised delineation of these domains. We present SpatialDG, a dual-graph self-supervised contrastive learning framework for ST. SpatialDG combines graph neural networks with self-supervised contrastive learning to learn informative and discriminative spot representations by maximizing the agreement between local (node) and global (graph) embeddings and leveraging spatial adjacency to enhance representation learning. Specifically, SpatialDG constructs both a gene expression similarity graph and a spatial adjacency graph, integrating them via a dual-view contrastive architecture that aligns molecular and spatial information, while a zero-inflated negative binomial reconstruction loss accounts for the count-based and sparse nature of gene expression data. SpatialDG achieves significant gains over state-of-the-art algorithms in both healthy and cancer datasets, demonstrating robust generalization across diverse ST landscapes. In conclusion, SpatialDG efficiently unravels biologically meaningful domains from spatial and genetic signals, providing a powerful and generalizable tool to mine tissue architecture in ST datasets.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.