Integrating Multiple Single-Cell RNA Sequencing Datasets Using Adversarial Autoencoders

Author:

Wang Xun1ORCID,Zhang Chaogang1ORCID,Wang Lulu1,Zheng Pan2ORCID

Affiliation:

1. College of Computer Science and Technology, China University of Petroleum East China, Qingdao 266580, China

2. Department of Accounting and Information Systems, University of Canterbury, Christchurch 8041, New Zealand

Abstract

Single-cell RNA sequencing (RNA-seq) has been demonstrated to be a proven method for quantifying gene-expression heterogeneity and providing insight into the transcriptome at the single-cell level. When combining multiple single-cell transcriptome datasets for analysis, it is common to first correct the batch effect. Most of the state-of-the-art processing methods are unsupervised, i.e., they do not utilize single-cell cluster labeling information, which could improve the performance of batch correction methods, especially in the case of multiple cell types. To better utilize known labels for complex dataset scenarios, we propose a novel deep learning model named IMAAE (i.e., integrating multiple single-cell datasets via an adversarial autoencoder) to correct the batch effects. After conducting experiments with various dataset scenarios, the results show that IMAAE outperforms existing methods for both qualitative measures and quantitative evaluation. In addition, IMAAE is able to retain both corrected dimension reduction data and corrected gene expression data. These features make it a potential new option for large-scale single-cell gene expression data analysis.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. DeepDualEPI: Predicting Promoter-Enhancer Interactions Based on DNA Sequence and Genomic Signals;2023 IEEE International Conference on Bioinformatics and Biomedicine (BIBM);2023-12-05

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