Evidence map›Paper›PMID 39804726›Full record

ArticleGigaScience2025

Unveiling patterns in spatial transcriptomics data: a novel approach utilizing graph attention autoencoder and multiscale deep subspace clustering network.

Liqian Zhou, Xinhuai Peng, Min Chen, Xianzhi He, Geng Tian, Jialiang Yang, Lihong Peng

Abstract read
In one paragraph

Article in GigaScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Article
  9. Artificial Intelligence Revolution in Transcriptomics: From Single Cells to Spatial Atlases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Liqian ZhouSchool of Computer Science, Hunan University of Technology, Zhuzhou 412007, Hunan, China.
Xinhuai PengSchool of Computer Science, Hunan University of Technology, Zhuzhou 412007, Hunan, China.
Min ChenSchool of Computer Science, Hunan Institute of Technology, Hengyang 421002, Hunan, China.
Xianzhi HeSchool of Computer Science, Hunan University of Technology, Zhuzhou 412007, Hunan, China.
Geng TianGeneis (Beijing) Co. Ltd., Beijing 100102, China.ORCID 0000-0001-5752-4436
Jialiang YangGeneis (Beijing) Co. Ltd., Beijing 100102, China.ORCID 0000-0003-4689-8672
Lihong PengSchool of Computer Science, Hunan University of Technology, Zhuzhou 412007, Hunan, China.ORCID 0000-0002-2321-3901

Funding

National Natural Science Foundation of China 62072172Natural Science Foundation of Hunan Province 2021JJ30219
6 · The paper itself

Abstract

backgroundThe accurate deciphering of spatial domains, along with the identification of differentially expressed genes and the inference of cellular trajectory based on spatial transcriptomic (ST) data, holds significant potential for enhancing our understanding of tissue organization and biological functions. However, most of spatial clustering methods can neither decipher complex structures in ST data nor entirely employ features embedded in different layers.

resultsThis article introduces STMSGAL, a novel framework for analyzing ST data by incorporating graph attention autoencoder and multiscale deep subspace clustering. First, STMSGAL constructs ctaSNN, a cell type-aware shared nearest neighbor graph, using Louvian clustering exclusively based on gene expression profiles. Subsequently, it integrates expression profiles and ctaSNN to generate spot latent representations using a graph attention autoencoder and multiscale deep subspace clustering. Lastly, STMSGAL implements spatial clustering, differential expression analysis, and trajectory inference, providing comprehensive capabilities for thorough data exploration and interpretation. STMSGAL was evaluated against 7 methods, including SCANPY, SEDR, CCST, DeepST, GraphST, STAGATE, and SiGra, using four 10x Genomics Visium datasets, 1 mouse visual cortex STARmap dataset, and 2 Stereo-seq mouse embryo datasets. The comparison showcased STMSGAL's remarkable performance across Davies-Bouldin, Calinski-Harabasz, S_Dbw, and ARI values. STMSGAL significantly enhanced the identification of layer structures across ST data with different spatial resolutions and accurately delineated spatial domains in 2 breast cancer tissues, adult mouse brain (FFPE), and mouse embryos.

conclusionsSTMSGAL can serve as an essential tool for bridging the analysis of cellular spatial organization and disease pathology, offering valuable insights for researchers in the field.

Indexed as

AutoencoderComputational BiologyGene Expression ProfilingTranscriptomeAlgorithmsAnimalsCluster AnalysisHumansMiceSoftwarecell type–aware spatial neighbor networkdeep subspace clusteringdifferential expression analysisgraph attention autoencoderlatent embedding feature learningmultiscale self-expressionself-supervised learningspatial transcriptomicstrajectory inference

Identifiers

PMID39804726
PMCPMC11727722

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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.