scMultiGAN: cell-specific imputation for single-cell transcriptomes with multiple deep generative adversarial networks

Author:

Wang Tao123,Zhao Hui4,Xu Yungang56,Wang Yongtian123,Shang Xuequn123,Peng Jiajie123,Xiao Bing4

Affiliation:

1. School of Computer Science, Northwestern Polytechnical University , 1 Dongxiang Rd., 710072 Xi’an , China

2. Key Laboratory of Big Data Storage and Management , Ministry of Industry and Information Technology, , 1 Dongxiang Rd., 710072 Xi’an , China

3. Northwestern Polytechnical University , Ministry of Industry and Information Technology, , 1 Dongxiang Rd., 710072 Xi’an , China

4. School of Automation, Northwestern Polytechnical University , 1 Dongxiang Rd., 710072 Xi’an , China

5. Department of Cell Biology and Genetics , School of Basic Medical Sciences, Xi’an , No.28, West Xianning Road, 710061 Xi’an , China

6. Jiaotong University Health Science Center , School of Basic Medical Sciences, Xi’an , No.28, West Xianning Road, 710061 Xi’an , China

Abstract

Abstract The emergence of single-cell RNA sequencing (scRNA-seq) technology has revolutionized the identification of cell types and the study of cellular states at a single-cell level. Despite its significant potential, scRNA-seq data analysis is plagued by the issue of missing values. Many existing imputation methods rely on simplistic data distribution assumptions while ignoring the intrinsic gene expression distribution specific to cells. This work presents a novel deep-learning model, named scMultiGAN, for scRNA-seq imputation, which utilizes multiple collaborative generative adversarial networks (GAN). Unlike traditional GAN-based imputation methods that generate missing values based on random noises, scMultiGAN employs a two-stage training process and utilizes multiple GANs to achieve cell-specific imputation. Experimental results show the efficacy of scMultiGAN in imputation accuracy, cell clustering, differential gene expression analysis and trajectory analysis, significantly outperforming existing state-of-the-art techniques. Additionally, scMultiGAN is scalable to large scRNA-seq datasets and consistently performs well across sequencing platforms. The scMultiGAN code is freely available at https://github.com/Galaxy8172/scMultiGAN.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Fundamental Research Funds for the Central Universities

Young Elite Scientists Sponsorship Program

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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