| Literature DB >> 34929734 |
Mario Flores1, Zhentao Liu1, Tinghe Zhang1, Md Musaddaqui Hasib1, Yu-Chiao Chiu2, Zhenqing Ye2,3, Karla Paniagua1, Sumin Jo1, Jianqiu Zhang1, Shou-Jiang Gao4,5, Yu-Fang Jin1, Yidong Chen2,3, Yufei Huang6,5.
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.Entities:
Keywords: batch correction; cell-type identificationfunctional prediction; clustering; deep learning; dimensionality reduction; imputation; single-cell RNA-seq; visualization
Mesh:
Year: 2022 PMID: 34929734 PMCID: PMC8769926 DOI: 10.1093/bib/bbab531
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 13.994