Evidence map›Paper›PMID 39717398›Full record

ArticleComputational and structural biotechnology journal2024

Deep clustering representation of spatially resolved transcriptomics data using multi-view variational graph auto-encoders with consensus clustering.

Jinyun Niu, Fangfang Zhu, Taosheng Xu, Shunfang Wang, Wenwen Min

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Article in Computational and structural biotechnology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Computer Vision Methods for Spatial Transcriptomics: A Survey.bioRxiv : the preprint server for biology · 2025
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jinyun NiuSchool of Information Science and Engineering, Yunnan University, Kunming, 650091, Yunnan, China.
Fangfang ZhuSchool of Health and Nursing, Yunnan Open University, Kunming, 650599, Yunnan, China.
Taosheng XuHefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, 230031, Anhui, China.
Shunfang WangSchool of Information Science and Engineering, Yunnan University, Kunming, 650091, Yunnan, China.
Wenwen MinSchool of Information Science and Engineering, Yunnan University, Kunming, 650091, Yunnan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapid development of spatial transcriptomics (ST) technology has provided unprecedented opportunities to understand tissue relationships and functions within specific spatial contexts. Accurate identification of spatial domains is crucial for downstream spatial transcriptomics analysis. However, effectively combining gene expression data, histological images and spatial coordinate data to identify spatial domains remains a challenge. To this end, we propose STMVGAE, a novel spatial transcriptomics analysis tool that combines a multi-view variational graph autoencoder with a consensus clustering framework. STMVGAE begins by extracting histological images features using a pre-trained convolutional neural network (CNN) and integrates these features with gene expression data to generate augmented gene expression profiles. Subsequently, multiple graphs (views) are constructed using various similarity measures, capturing different aspects of the spatial and transcriptional relationships. These views, combined with the augmented gene expression data, are then processed through variational graph auto-encoders (VGAEs) to learn multiple low-dimensional latent embeddings. Finally, the model employs a consensus clustering method to integrate the clustering results derived from these embeddings, significantly improving clustering accuracy and stability. We applied STMVGAE to five real datasets and compared it with five state-of-the-art methods, showing that STMVGAE consistently achieves competitive results. We assessed its capabilities in spatial domain identification and evaluated its performance across various downstream tasks, including UMAP visualization, PAGA trajectory inference, spatially variable gene (SVG) identification, denoising, batch integration, and other analyses. All code and public datasets used in this paper is available at https://github.com/wenwenmin/STMVGAE and https://zenodo.org/records/13119867.

Indexed as

Consensus clusteringDeep learningMulti-view variational graph autoencodersSpatially resolved transcriptomics

Identifiers

PMID39717398
PMCPMC11664090

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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 OpenQuestion graph.