scMAE: a masked autoencoder for single-cell RNA-seq clustering

被引:7
|
作者
Fang, Zhaoyu [1 ]
Zheng, Ruiqing [1 ]
Li, Min [1 ]
机构
[1] Cent South Univ, Sch Comp Sci & Engn, 932 South Lushan Rd, Changsha 410083, Peoples R China
基金
中国国家自然科学基金;
关键词
HETEROGENEITY; MODEL;
D O I
10.1093/bioinformatics/btae020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation Single-cell RNA sequencing has emerged as a powerful technology for studying gene expression at the individual cell level. Clustering individual cells into distinct subpopulations is fundamental in scRNA-seq data analysis, facilitating the identification of cell types and exploration of cellular heterogeneity. Despite the recent development of many deep learning-based single-cell clustering methods, few have effectively exploited the correlations among genes, resulting in suboptimal clustering outcomes.Results Here, we propose a novel masked autoencoder-based method, scMAE, for cell clustering. scMAE perturbs gene expression and employs a masked autoencoder to reconstruct the original data, learning robust and informative cell representations. The masked autoencoder introduces a masking predictor, which captures relationships among genes by predicting whether gene expression values are masked. By integrating this masking mechanism, scMAE effectively captures latent structures and dependencies in the data, enhancing clustering performance. We conducted extensive comparative experiments using various clustering evaluation metrics on 15 scRNA-seq datasets from different sequencing platforms. Experimental results indicate that scMAE outperforms other state-of-the-art methods on these datasets. In addition, scMAE accurately identifies rare cell types, which are challenging to detect due to their low abundance. Furthermore, biological analyses confirm the biological significance of the identified cell subpopulations.Availability and implementation The source code of scMAE is available at: https://zenodo.org/records/10465991.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] scVGATAE: A Variational Graph Attentional Autoencoder Model for Clustering Single-Cell RNA-seq Data
    Liu, Lijun
    Wu, Xiaoyang
    Yu, Jun
    Zhang, Yuduo
    Niu, Kaixing
    Yu, Anli
    BIOLOGY-BASEL, 2024, 13 (09):
  • [2] Single-cell RNA-seq denoising using a deep count autoencoder
    Gökcen Eraslan
    Lukas M. Simon
    Maria Mircea
    Nikola S. Mueller
    Fabian J. Theis
    Nature Communications, 10
  • [3] AutoImpute: Autoencoder based imputation of single-cell RNA-seq data
    Divyanshu Talwar
    Aanchal Mongia
    Debarka Sengupta
    Angshul Majumdar
    Scientific Reports, 8
  • [4] AutoImpute: Autoencoder based imputation of single-cell RNA-seq data
    Talwar, Divyanshu
    Mongia, Aanchal
    Sengupta, Debarka
    Majumdar, Angshul
    SCIENTIFIC REPORTS, 2018, 8
  • [5] Single-cell RNA-seq denoising using a deep count autoencoder
    Eraslan, Goekcen
    Simon, Lukas M.
    Mircea, Maria
    Mueller, Nikola S.
    Theis, Fabian J.
    NATURE COMMUNICATIONS, 2019, 10 (1)
  • [6] Bubble: a fast single-cell RNA-seq imputation using an autoencoder constrained by bulk RNA-seq data
    Chen, Siqi
    Yan, Xuhua
    Zheng, Ruiqing
    Li, Min
    BRIEFINGS IN BIOINFORMATICS, 2023, 24 (01)
  • [7] Analysis of Single-Cell RNA-seq Data by Clustering Approaches
    Zhu, Xiaoshu
    Li, Hong-Dong
    Guo, Lilu
    Wu, Fang-Xiang
    Wang, Jianxin
    CURRENT BIOINFORMATICS, 2019, 14 (04) : 314 - 322
  • [8] scGMAI: a Gaussian mixture model for clustering single-cell RNA-Seq data based on deep autoencoder
    Yu, Bin
    Chen, Chen
    Qi, Ren
    Zheng, Ruiqing
    Skillman-Lawrence, Patrick J.
    Wang, Xiaolin
    Ma, Anjun
    Gu, Haiming
    BRIEFINGS IN BIOINFORMATICS, 2021, 22 (04)
  • [9] An interpretable framework for clustering single-cell RNA-Seq datasets
    Jesse M. Zhang
    Jue Fan
    H. Christina Fan
    David Rosenfeld
    David N. Tse
    BMC Bioinformatics, 19
  • [10] Challenges in unsupervised clustering of single-cell RNA-seq data
    Kiselev, Vladimir Yu
    Andrews, Tallulah S.
    Hemberg, Martin
    NATURE REVIEWS GENETICS, 2019, 20 (05) : 273 - 282