ArticlePLoS computational biology2025
SpaMWGDA: Identifying spatial domains of spatial transcriptomes using multi-view weighted fusion graph convolutional network and data augmentation.
Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.
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
1 citing paper in PubMed.
- Correction: SpaMWGDA: Identifying spatial domains of spatial transcriptomes using multi-view weighted fusion graph convolutional network and data augmentation.PLoS computational biology · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
6 authors.
Funding
Abstract
The rapid development of spatial transcriptomics (ST) has made it possible to effectively integrate gene expression and spatial information of cells and accurately identify spatial domains. A large number of deep learning (DL)-based methods have been proposed to perform spatial domain identification and achieved impressive results. However, these methods have some limitations. First, these methods rely on a fixed similarity metric and cannot fully utilize neighborhood information. Second, they cannot efficiently and adaptively integrate key information when fusing and reconstructing gene expression using purely additive methods. Finally, these methods ignore key nonlinear features and introduce noise during clustering. To address these limitations, we propose a novel DL model SpaMWGDA based on multi-view weighted fused graph convolutional network (GCN) and data augmentation. By modeling spatial information using different similarity metrics, the model is able to successfully capture comprehensive neighborhood information of the spot features. By combining data augmentation and contrastive learning, SpaMWGDA is able to learn key gene expressions. SpaMWGDA uses a multi-view GCN encoder to model the similarities between spatial information and gene features, and uses a view-level attention mechanism for weighted fusion to adaptively learn the dependencies between them and learn the key features of each view. Experimental results not only demonstrate that SpaMWGDA outperforms competing methods in spatial domain identification and trajectory inference but also show the ability of SpaMWGDA to analyse tissue structure and function. The source code for SpaMWGDA is available at https://github.com/nathanyl/SpaMWGDA .
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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.