ArticleGenomics, proteomics & bioinformatics2026
DisConST: Distribution-aware Contrastive Learning for Spatial Domain Identification.
Article in Genomics, proteomics & bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed.
- Φ-Space ST: A platform-agnostic method to identify cell states in spatial transcriptomics studies.Cell reports methods · 2026Article
- Structural-information guided fusion for spatial domain identification from spatial transcriptomics.Bioinformatics (Oxford, England) · 2026Article
- Knowledge-graph-enhanced multi-scale modeling for drug-drug interaction prediction.Molecular therapy. Nucleic acids · 2026Article
- stSCI: A multi-task learning framework for integrative analysis of single-cell and spatial transcriptomics data.Innovation (Cambridge (Mass.)) · 2026Article
- STGNET: extending panel coverage in imaging-based spatial transcriptomics using deep generative adversarial networks.Briefings in bioinformatics · 2026Article
- Single-cell Spatial Multiomics: Technologies, Methods, and Biological Applications.Genomics, proteomics & bioinformatics · 2026Article
- Signal-based spatial domain identification of spatially resolved transcriptomics with multigraph fusion.Briefings in bioinformatics · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
Spatial transcriptomics (ST) is a cutting-edge technology that provides comprehensive insights into gene expression (GE) patterns from a spatial perspective. A key research focus within this field is spatial domain identification, which is essential for exploring tissue organization, biological development, and disease mechanisms. Although methods have been developed, they still face challenges in modeling GE information together with spatial locations, resulting in suboptimal accuracy. Here, we introduce Distribution-aware Contrastive Learning for Spatial Transcriptomics (DisConST), a novel deep learning method designed to improve spatial domain detection within ST datasets. DisConST addresses key challenges, such as the high dropout rates and the complex integration of spatial and GE data, by incorporating contrastive learning strategies that are aware of the underlying data distributions. It employs the zero-inflated negative binomial distribution, along with graph contrastive learning, to generate more informative latent representations. These representations efficiently integrate spatial positions, transcriptomic profiles, and cell-type proportions within spots. We validated DisConST across diverse ST datasets of tissues, organs, and embryos from various sequencing platforms in both normal and disease states. Our results consistently demonstrate that DisConST achieves superior spatial domain recognition accuracy compared to existing state-of-the-art methods. Furthermore, our experiments highlight the utility of DisConST in advancing research on tissue organization, embryonic development, and tumor immune microenvironment dissection. The source code for DisConST is freely available at https://github.com/Zhenpm/DisConST/.
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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.