Evidence map›Paper›PMID 40511990›Full record

ArticleBioinformatics (Oxford, England)2025

Differentiable graph clustering with structural grouping for single-cell RNA-seq data.

Xiaoqiang Yan, Shike Du, Quan Zou, Zhen Tian

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiaoqiang YanSchool of Computer and Artificial Intelligence, Zhengzhou University, Zhengzhou 450000, China.
Shike DuSchool of Computer and Artificial Intelligence, Zhengzhou University, Zhengzhou 450000, China.
Quan ZouYangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou 324000, China.ORCID 0000-0001-6406-1142
Zhen TianSchool of Computer and Artificial Intelligence, Zhengzhou University, Zhengzhou 450000, China.ORCID 0000-0003-0945-8168

Funding

Municipal Government of Quzhou 2024D033National Natural Science Foundation of China 62131004National Natural Science Foundation of China 62371423Natural Science Foundation of Henan 252300421226Natural Science Foundation of Henan 252300421504
6 · The paper itself

Abstract

motivationClustering cells into subpopulations is one of the most crucial tasks in single-cell RNA sequencing (scRNA-seq) data analysis, which provides support for biological research at cellular level. With the development of graph neural networks, deep graph clustering approaches have achieved excellent performance by modeling the topological relationships between cells. However, existing approaches rely on cell node and its neighbors to obtain the cell feature representation, which ignore the graph cluster structure hidden in scRNA-seq data. Besides, how to bridge the heterogeneous gap between cell node feature and its structural information remains a highly challenging problem.

resultsHere, we propose a novel differentiable graph clustering with structural grouping (DGCSG) for scRNA-seq data, which incorporates graph cluster information into deep graph clustering model by designing a differentiable clustering mechanism to learn clustering-friendly representation. Firstly, an interactive module is devised to dynamically transfer node representations learned by autoencoder (AE) to graph attention autoencoder (GATE) in layer-by-layer manner. Then, to characterize graph cluster information, a differentiable clustering mechanism is proposed to transform K-way normalized cuts from a discrete optimization problem into differentiable learning objective through spectral relaxation, which jointly optimizes the GATE by allocating more attention scores to nodes in the same graph cluster. Finally, a decoupled self-supervised optimization is proposed, which guides the representation learning of AE and GATE in the interactive module. Extensive evaluations on 14 scRNA-seq benchmarks verify the superiority of DGCSG compared with state-of-the-art baselines. AVAILABILITY AND IMPLEMENTATION: The code associated with this work is available on GitHub (https://github.com/Xiaoqiang-Yan/DGCSG).

Indexed as

RNA-SeqSequence Analysis, RNASingle-Cell AnalysisAlgorithmsCluster AnalysisComputational BiologyHumansNeural Networks, ComputerSingle-Cell Gene Expression Analysis

Identifiers

PMID40511990
PMCPMC12212642

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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.