Deep learning tackles single-cell analysis—a survey of deep learning for scRNA-seq analysis

Author:

Flores Mario1ORCID,Liu Zhentao1,Zhang Tinghe1,Hasib Md Musaddaqui1,Chiu Yu-Chiao2ORCID,Ye Zhenqing23,Paniagua Karla1,Jo Sumin1,Zhang Jianqiu1,Gao Shou-Jiang45,Jin Yu-Fang1,Chen Yidong23,Huang Yufei65

Affiliation:

1. Department of Electrical and Computer Engineering, the University of Texas at San Antonio, San Antonio, TX 78249, USA

2. Greehey Children’s Cancer Research Institute, University of Texas Health San Antonio, San Antonio, TX 78229, USA

3. Department of Population Health Sciences, University of Texas Health San Antonio, San Antonio, TX 78229, USA

4. Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania, PA 15232, USA

5. UPMC Hillman Cancer Center, University of Pittsburgh, PA 15232, USA

6. Department of Medicine, School of Medicine, University of Pittsburgh, PA 15232, USA

Abstract

Abstract Since its selection as the method of the year in 2013, single-cell technologies have become mature enough to provide answers to complex research questions. With the growth of single-cell profiling technologies, there has also been a significant increase in data collected from single-cell profilings, resulting in computational challenges to process these massive and complicated datasets. To address these challenges, deep learning (DL) is positioned as a competitive alternative for single-cell analyses besides the traditional machine learning approaches. Here, we survey a total of 25 DL algorithms and their applicability for a specific step in the single cell RNA-seq processing pipeline. Specifically, we establish a unified mathematical representation of variational autoencoder, autoencoder, generative adversarial network and supervised DL models, compare the training strategies and loss functions for these models, and relate the loss functions of these models to specific objectives of the data processing step. Such a presentation will allow readers to choose suitable algorithms for their particular objective at each step in the pipeline. We envision that this survey will serve as an important information portal for learning the application of DL for scRNA-seq analysis and inspire innovative uses of DL to address a broader range of new challenges in emerging multi-omics and spatial single-cell sequencing.

Funder

National Institutes of Health

NCI Cancer Center Shared Resources

National Science Foundation

Cancer Prevention and Research Institute of Texas

Fund for Innovation in Cancer Informatics

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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