基于深度传递图卷积网络的非配对单细胞组学数据集成。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2025-01-16 eCollection Date: 2025-01-01 DOI:10.1371/journal.pcbi.1012625
Yulong Kan, Yunjing Qi, Zhongxiao Zhang, Xikeng Liang, Weihao Wang, Shuilin Jin
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引用次数: 0

摘要

大规模图谱水平的单细胞RNA序列和单细胞染色质可及性数据的快速发展为广泛而深入地了解复杂的生物学机制提供了非凡的途径。利用这些数据集并将标签从scRNA-seq转移到scATAC-seq将使单细胞组学数据的探索成为可能。然而,目前的标签转移方法性能有限,主要是由于保存细粒度细胞群和数据集之间内在或外在异质性的能力较低。在这里,我们提出了一种基于深度转移模型的鲁棒图卷积网络scTGCN,它在保存生物变异方面实现了多种性能,同时在几分钟内以低内存消耗实现了数十万个细胞的整合。我们发现scTGCN对于整合小鼠图谱数据和由APSA-seq和CITE-seq生成的多模态数据具有强大的功能。因此,scTGCN具有较高的标签转移准确性和跨模式的有效知识转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integration of unpaired single cell omics data by deep transfer graph convolutional network.

The rapid advance of large-scale atlas-level single cell RNA sequences and single-cell chromatin accessibility data provide extraordinary avenues to broad and deep insight into complex biological mechanism. Leveraging the datasets and transfering labels from scRNA-seq to scATAC-seq will empower the exploration of single-cell omics data. However, the current label transfer methods have limited performance, largely due to the lower capable of preserving fine-grained cell populations and intrinsic or extrinsic heterogeneity between datasets. Here, we present a robust deep transfer model based graph convolutional network, scTGCN, which achieves versatile performance in preserving biological variation, while achieving integration hundreds of thousands cells in minutes with low memory consumption. We show that scTGCN is powerful to the integration of mouse atlas data and multimodal data generated from APSA-seq and CITE-seq. Thus, scTGCN shows high label transfer accuracy and effectively knowledge transfer across different modalities.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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