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

Journal: Briefings in bioinformatics
Published Date:

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.

Authors

  • Mario Flores
    Department of Electrical and Computer Engineering, The University of Texas at San Antonio, San Antonio, TX, 78249-0669, USA. Electronic address: mario.flores@utsa.edu.
  • Zhentao Liu
  • Tinghe Zhang
    Department of Electrical and Computer Engineering, The University of Texas at San Antonio, San Antonio, TX, 78249, USA.
  • Md Musaddaqui Hasib
    Department of Electrical and Computer Engineering, the University of Texas at San Antonio, San Antonio, TX 78249, USA.
  • Yu-Chiao Chiu
    Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.
  • Zhenqing Ye
    Greehey Children's Cancer Research Institute, University of Texas Health San Antonio, San Antonio, TX 78229, USA.
  • Karla Paniagua
    Department of Electrical and Computer Engineering, the University of Texas at San Antonio, San Antonio, TX 78249, USA.
  • Sumin Jo
    Department of Electronic and Electrical Engineering, Ewha Womans University, 11-1 Daehyun-Dong, Seodaemoon-Gu, Seoul 03760, Republic of Korea.
  • Jianqiu Zhang
    Department of Electrical and Computer Engineering, the University of Texas at San Antonio, San Antonio, TX 78249, USA.
  • Shou-Jiang Gao
    Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, Pennsylvania, PA 15232, USA.
  • Yu-Fang Jin
  • Yidong Chen
    Greehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA. ChenY8@uthscsa.edu.
  • Yufei Huang
    Department of Electrical and Computer Engineering, The University of Texas at San Antonio, San Antonio, TX, 78249, USA.