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scDTL:通过利用批量细胞信息进行深度迁移学习增强单细胞 RNA-seq 推断。

scDTL: enhancing single-cell RNA-seq imputation through deep transfer learning with bulk cell information.

机构信息

College of Computer Science and Software Engineering, Shenzhen University, Guangdong 518057, China.

College of Future Technology, HKUST(GZ), Guangdong 510641, China.

出版信息

Brief Bioinform. 2024 Sep 23;25(6). doi: 10.1093/bib/bbae555.

DOI:10.1093/bib/bbae555
PMID:39504481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11540133/
Abstract

The increasing single-cell RNA sequencing (scRNA-seq) data enable researchers to explore cellular heterogeneity and gene expression profiles, offering a high-resolution view of the transcriptome at the single-cell level. However, the dropout events, which are often present in scRNA-seq data, remaining challenges for downstream analysis. Although a number of studies have been developed to recover single-cell expression profiles, their performance may be hindered due to not fully exploring the inherent relations between genes. To address the issue, we propose scDTL, a deep transfer learning based approach for scRNA-seq data imputation by harnessing the bulk RNA-sequencing information. We firstly employ a denoising autoencoder trained on bulk RNA-seq data as the initial imputation model, and then leverage a domain adaptation framework that transfers the knowledge learned by the bulk imputation model to scRNA-seq learning task. In addition, scDTL employs a parallel operation with a 1D U-Net denoising model to provide gene representations of varying granularity, capturing both coarse and fine features of the scRNA-seq data. Finally, we utilize a cross-channel attention mechanism to fuse the features learned from the transferred bulk imputation model and U-Net model. In the evaluation, we conduct extensive experiments to demonstrate that scDTL could outperform other state-of-the-art methods in the quantitative comparison and downstream analyses.

摘要

单细胞 RNA 测序 (scRNA-seq) 数据的不断增加,使研究人员能够探索细胞异质性和基因表达谱,提供单细胞水平转录组的高分辨率视图。然而,在 scRNA-seq 数据中经常存在的缺失事件仍然是下游分析的挑战。尽管已经有许多研究致力于恢复单细胞表达谱,但由于未能充分挖掘基因之间的内在关系,其性能可能会受到阻碍。为了解决这个问题,我们提出了 scDTL,这是一种基于深度迁移学习的方法,通过利用批量 RNA-seq 信息来进行 scRNA-seq 数据插补。我们首先使用在批量 RNA-seq 数据上训练的去噪自动编码器作为初始插补模型,然后利用域自适应框架将批量插补模型学习到的知识转移到 scRNA-seq 学习任务中。此外,scDTL 采用并行操作,使用 1D U-Net 去噪模型提供不同粒度的基因表示,同时捕获 scRNA-seq 数据的粗粒度和细粒度特征。最后,我们利用交叉通道注意力机制融合从转移的批量插补模型和 U-Net 模型中学习到的特征。在评估中,我们进行了广泛的实验,以证明 scDTL 在定量比较和下游分析中可以优于其他最先进的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/5ebba1422135/bbae555f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/f77593774584/bbae555f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/882361c9cbb7/bbae555f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/40f347121a7d/bbae555f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/cd892d06e565/bbae555f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/5ebba1422135/bbae555f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/f77593774584/bbae555f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/6b6a8b96803e/bbae555f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/882361c9cbb7/bbae555f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/40f347121a7d/bbae555f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/cd892d06e565/bbae555f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f383/11540133/5ebba1422135/bbae555f6.jpg

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本文引用的文献

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CL-Impute: A contrastive learning-based imputation for dropout single-cell RNA-seq data.CL-Impute:基于对比学习的 dropout 单细胞 RNA-seq 数据插补方法。
Comput Biol Med. 2023 Sep;164:107263. doi: 10.1016/j.compbiomed.2023.107263. Epub 2023 Jul 23.
2
Deep single-cell RNA-seq data clustering with graph prototypical contrastive learning.基于图原型对比学习的深度单细胞 RNA-seq 数据聚类。
Bioinformatics. 2023 Jun 1;39(6). doi: 10.1093/bioinformatics/btad342.
3
scGCL: an imputation method for scRNA-seq data based on graph contrastive learning.
scGCL:一种基于图对比学习的 scRNA-seq 数据插补方法。
Bioinformatics. 2023 Mar 1;39(3). doi: 10.1093/bioinformatics/btad098.
4
scGGAN: single-cell RNA-seq imputation by graph-based generative adversarial network.scGGAN:基于图的生成对抗网络的单细胞RNA测序数据插补
Brief Bioinform. 2023 Mar 19;24(2). doi: 10.1093/bib/bbad040.
5
scDCCA: deep contrastive clustering for single-cell RNA-seq data based on auto-encoder network.scDCCA:基于自动编码器网络的单细胞RNA测序数据深度对比聚类
Brief Bioinform. 2023 Jan 19;24(1). doi: 10.1093/bib/bbac625.
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Deep transfer learning of cancer drug responses by integrating bulk and single-cell RNA-seq data.通过整合 bulk 和单细胞 RNA-seq 数据进行癌症药物反应的深度迁移学习。
Nat Commun. 2022 Oct 30;13(1):6494. doi: 10.1038/s41467-022-34277-7.
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GE-Impute: graph embedding-based imputation for single-cell RNA-seq data.GE-Impute:基于图嵌入的单细胞 RNA-seq 数据插补。
Brief Bioinform. 2022 Sep 20;23(5). doi: 10.1093/bib/bbac313.
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A Bayesian factorization method to recover single-cell RNA sequencing data.一种贝叶斯因子分解方法,用于恢复单细胞 RNA 测序数据。
Cell Rep Methods. 2021 Dec 20;2(1):100133. doi: 10.1016/j.crmeth.2021.100133. eCollection 2022 Jan 24.
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Imputing single-cell RNA-seq data by combining graph convolution and autoencoder neural networks.通过结合图卷积和自动编码器神经网络对单细胞RNA测序数据进行插补
iScience. 2021 Apr 2;24(5):102393. doi: 10.1016/j.isci.2021.102393. eCollection 2021 May 21.
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scGNN is a novel graph neural network framework for single-cell RNA-Seq analyses.scGNN 是一种用于单细胞 RNA-Seq 分析的新型图神经网络框架。
Nat Commun. 2021 Mar 25;12(1):1882. doi: 10.1038/s41467-021-22197-x.