Graph contrastive learning as a versatile foundation for advanced scRNA-seq data analysis.

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Briefings in bioinformatics Pub Date : 2024-09-23 DOI:10.1093/bib/bbae558
Zhenhao Zhang, Yuxi Liu, Meichen Xiao, Kun Wang, Yu Huang, Jiang Bian, Ruolin Yang, Fuyi Li
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Abstract

Single-cell RNA sequencing (scRNA-seq) offers unprecedented insights into transcriptome-wide gene expression at the single-cell level. Cell clustering has been long established in the analysis of scRNA-seq data to identify the groups of cells with similar expression profiles. However, cell clustering is technically challenging, as raw scRNA-seq data have various analytical issues, including high dimensionality and dropout values. Existing research has developed deep learning models, such as graph machine learning models and contrastive learning-based models, for cell clustering using scRNA-seq data and has summarized the unsupervised learning of cell clustering into a human-interpretable format. While advances in cell clustering have been profound, we are no closer to finding a simple yet effective framework for learning high-quality representations necessary for robust clustering. In this study, we propose scSimGCL, a novel framework based on the graph contrastive learning paradigm for self-supervised pretraining of graph neural networks. This framework facilitates the generation of high-quality representations crucial for cell clustering. Our scSimGCL incorporates cell-cell graph structure and contrastive learning to enhance the performance of cell clustering. Extensive experimental results on simulated and real scRNA-seq datasets suggest the superiority of the proposed scSimGCL. Moreover, clustering assignment analysis confirms the general applicability of scSimGCL, including state-of-the-art clustering algorithms. Further, ablation study and hyperparameter analysis suggest the efficacy of our network architecture with the robustness of decisions in the self-supervised learning setting. The proposed scSimGCL can serve as a robust framework for practitioners developing tools for cell clustering. The source code of scSimGCL is publicly available at https://github.com/zhangzh1328/scSimGCL.

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图形对比学习是高级 scRNA-seq 数据分析的多功能基础。
单细胞 RNA 测序(scRNA-seq)可在单细胞水平上深入了解整个转录组的基因表达。细胞聚类在 scRNA-seq 数据分析中早已确立,用于识别具有相似表达谱的细胞群。然而,细胞聚类在技术上具有挑战性,因为原始 scRNA-seq 数据存在各种分析问题,包括高维度和丢弃值。现有研究已经开发出了利用 scRNA-seq 数据进行细胞聚类的深度学习模型,如图机器学习模型和基于对比学习的模型,并将细胞聚类的无监督学习总结为人类可理解的格式。虽然在细胞聚类方面取得了长足的进步,但我们还没有找到一个简单而有效的框架来学习稳健聚类所需的高质量表征。在本研究中,我们提出了 scSimGCL,这是一个基于图对比学习范式的新型框架,用于图神经网络的自我监督预训练。该框架有助于生成对细胞聚类至关重要的高质量表征。我们的 scSimGCL 结合了细胞-细胞图结构和对比学习,以提高细胞聚类的性能。在模拟和真实 scRNA-seq 数据集上的大量实验结果表明了所提出的 scSimGCL 的优越性。此外,聚类赋值分析证实了 scSimGCL 的普遍适用性,包括最先进的聚类算法。此外,消融研究和超参数分析表明,我们的网络架构在自我监督学习设置中具有决策稳健性的功效。对于开发细胞聚类工具的从业人员来说,所提出的 scSimGCL 可以作为一个稳健的框架。scSimGCL 的源代码可在 https://github.com/zhangzh1328/scSimGCL 公开获取。
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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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