自编码
计算机科学
人工智能
深度学习
仿形(计算机编程)
机器学习
管道(软件)
生成语法
介绍(产科)
对抗制
数据科学
数据挖掘
医学
操作系统
放射科
程序设计语言
作者
Mario Flores,Zhentao Liu,Tinghe Zhang,Md Musaddaqui Hasib,Yu‐Chiao Chiu,Zhenqing Ye,Karla Paniagua,Sumin Jo,Jianqiu Zhang,Shou‐Jiang Gao,Yufang Jin,Yidong Chen,Yufei Huang
摘要
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.
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