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Detecting cell type from single cell RNA sequencing based on deep bi-stochastic graph regularized matrix factorization

Wei Lan, View ORCID ProfileJianwei Chen, Qingfeng Chen, Jin Liu, Jianxin Wang, Yi-Ping Phoebe Chen
doi: https://doi.org/10.1101/2022.05.16.492212
Wei Lan
1School of Computer, Electronic and Information, Guangxi University, Nanning, Guangxi, 530004 and Hunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University, Changsha, Hunan, 410083, China. E-mail:
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  • For correspondence: lanwei@gxu.edu.cn
Jianwei Chen
2School of Computer, Electronic and Information, Guangxi University, Nanning, Guangxi, 530004, China. E-mail:
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  • For correspondence: jaychen.ooox@foxmail.com jaychen.ooox@foxmail.com
Qingfeng Chen
3School of Computer, Electronic and Information and State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi University, Nanning, Guangxi, 530004, China. E-mail:
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  • For correspondence: qingfeng@gxu.edu.cn
Jin Liu
4Hunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University, Changsha, Hunan, 410083, China. E-mail:
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  • For correspondence: liujin06@mail.csu.edu.cn
Jianxin Wang
5Hunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering, Central South University, Changsha, Hunan, 410083, China. E-mail:
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  • For correspondence: jxwang@mail.csu.edu.cn
Yi-Ping Phoebe Chen
6Department of Computer Science and Information Technology, La Trobe University, Melbourne Victoria 3086, Australia. E-mail:
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  • For correspondence: phoebe.chen@latrobe.edu.au
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Abstract

The application of fruitful achievement of single-cell RNA-sequencing (scRNA-seq) technology has generated huge amount of gene transcriptome data. It has provided a whole new perspective to analyze the transcriptome at single-cell level. Cluster analysis of scRNA-seq is an efficient approach to reveal unknown heterogeneity and functional diversity of cell populations, which could further assist researchers to explore pathogenesis and biomarkers of diseases. In this paper, we propose a new cluster method (DSINMF) based on deep matrix factorization to detect cell type in the scRNA-seq data. In our method, the feature selection is used to reduce redundant features. Then, the imputation method is utilized to impute dropout events. Further, the dimension reduction is utilized to reduce the impact of noise. Finally, the deep matrix factorization with bi-stochastic graph regularization is employed to cluster scRNA-seq data. To evaluate the performance of DSINMF, eight datasets are used as test sets in the experiment. The experimental results show DSINMF outperformances than other state-of-the-art methods in clustering performance.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://github.com/lanbiolab/DSINMF

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted May 18, 2022.
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Detecting cell type from single cell RNA sequencing based on deep bi-stochastic graph regularized matrix factorization
Wei Lan, Jianwei Chen, Qingfeng Chen, Jin Liu, Jianxin Wang, Yi-Ping Phoebe Chen
bioRxiv 2022.05.16.492212; doi: https://doi.org/10.1101/2022.05.16.492212
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Detecting cell type from single cell RNA sequencing based on deep bi-stochastic graph regularized matrix factorization
Wei Lan, Jianwei Chen, Qingfeng Chen, Jin Liu, Jianxin Wang, Yi-Ping Phoebe Chen
bioRxiv 2022.05.16.492212; doi: https://doi.org/10.1101/2022.05.16.492212

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