Evidence map›Paper›PMID 40366859›Full record

ArticleBriefings in bioinformatics2025

Decoupled GNNs based on multi-view contrastive learning for scRNA-seq data clustering.

Xiaoyan Yu, Yixuan Ren, Min Xia, Zhenqiu Shu, Liehuang Zhu

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Xiaoyan YuSchool of Computer Science and Technology, Beijing Institute of Technology, Zhongguancun South Street, Haidian, Beijing, 100081, China.
Yixuan RenFaculty of Information Engineering and Automation, Kunming University of Science and Technology, Jingming South Road, Chenggong, Kunming, Yunnan, 650500, China.
Min XiaFaculty of Information Engineering and Automation, Kunming University of Science and Technology, Jingming South Road, Chenggong, Kunming, Yunnan, 650500, China.
Zhenqiu ShuFaculty of Information Engineering and Automation, Kunming University of Science and Technology, Jingming South Road, Chenggong, Kunming, Yunnan, 650500, China.ORCID 0000-0001-5737-3383
Liehuang ZhuSchool of Cyberspace Science and Technology, Beijing Institute of Technology, Zhongguancun South Street, Haidian, Beijing, 100081, China.ORCID 0000-0003-3277-3887

Funding

Yunnan Provincial Major Science and Technology Special Plan Projects 202402AD080001
6 · The paper itself

Abstract

Clustering is pivotal in deciphering cellular heterogeneity in single-cell RNA sequencing (scRNA-seq) data. However, it suffers from several challenges in handling the high dimensionality and complexity of scRNA-seq data. Especially when employing graph neural networks (GNNs) for cell clustering, the dependencies between cells expand exponentially with the number of layers. This results in high computational complexity, negatively impacting the model's training efficiency. To address these challenges, we propose a novel approach, called decoupled GNNs, based on multi-view contrastive learning (scDeGNN), for scRNA-seq data clustering. Firstly, this method constructs two adjacency matrices to generate distinct views, and trains them using decoupled GNNs to derive the initial cell feature representations. These representations are then refined through a multilayer perceptron and a contrastive learning layer, ensuring the consistency and discriminability of the learned features. Finally, the learned representations are fused and applied to the cell clustering task. Extensive experimental results on nine real scRNA-seq datasets from various organisms and tissues show that the proposed scDeGNN method significantly outperforms other state-of-the-art scRNA-seq data clustering algorithms across multiple evaluation metrics.

Indexed as

Machine LearningNeural Networks, ComputerRNA-SeqSequence Analysis, RNASingle-Cell AnalysisAlgorithmsAnimalsCluster AnalysisComputational BiologyHumansSingle-Cell Gene Expression Analysisclusteringcontrastive learningdecoupledGNNsmulti-viewscRNA-seq data

Identifiers

PMID40366859
PMCPMC12077398

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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.