scDFC: A deep fusion clustering method for single-cell RNA-seq data

被引:16
|
作者
Hu, Dayu [1 ]
Liang, Ke [1 ]
Zhou, Sihang [2 ]
Tu, Wenxuan [3 ]
Liu, Meng [1 ]
Liu, Xinwang [1 ]
机构
[1] Natl Univ Def Technol, Changsha, Peoples R China
[2] Natl Univ Def Technol, Sch Comp, Changsha, Peoples R China
[3] Natl Univ Def Technol, Coll Comp, Changsha, Peoples R China
基金
国家重点研发计划;
关键词
single cell transcriptomics; clustering; fusion network; deep learning; TRANSCRIPTOMIC ANALYSIS; HETEROGENEITY; DIVERSITY;
D O I
10.1093/bib/bbad216
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Clustering methods have been widely used in single-cell RNA-seq data for investigating tumor heterogeneity. Since traditional clustering methods fail to capture the high-dimension methods, deep clustering methods have drawn increasing attention these years due to their promising strengths on the task. However, existing methods consider either the attribute information of each cell or the structure information between different cells. In other words, they cannot sufficiently make use of all of this information simultaneously. To this end, we propose a novel single-cell deep fusion clustering model, which contains two modules, i.e. an attributed feature clustering module and a structure-attention feature clustering module. More concretely, two elegantly designed autoencoders are built to handle both features regardless of their data types. Experiments have demonstrated the validity of the proposed approach, showing that it is efficient to fuse attributes, structure, and attention information on single-cell RNA-seq data. This work will be further beneficial for investigating cell subpopulations and tumor microenvironment. The Python implementation of our work is now freely available at .
引用
收藏
页数:9
相关论文
共 50 条
  • [31] How deep is enough in single-cell RNA-seq?
    Aaron M Streets
    Yanyi Huang
    [J]. Nature Biotechnology, 2014, 32 : 1005 - 1006
  • [32] How deep is enough in single-cell RNA-seq?
    Streets, Aaron M.
    Huang, Yanyi
    [J]. NATURE BIOTECHNOLOGY, 2014, 32 (10) : 1005 - 1006
  • [33] SCRABBLE: single-cell RNA-seq imputation constrained by bulk RNA-seq data
    Peng, Tao
    Zhu, Qin
    Yin, Penghang
    Tan, Kai
    [J]. GENOME BIOLOGY, 2019, 20 (1)
  • [34] SCRABBLE: single-cell RNA-seq imputation constrained by bulk RNA-seq data
    Tao Peng
    Qin Zhu
    Penghang Yin
    Kai Tan
    [J]. Genome Biology, 20
  • [35] An interpretable framework for clustering single-cell RNA-Seq datasets
    Jesse M. Zhang
    Jue Fan
    H. Christina Fan
    David Rosenfeld
    David N. Tse
    [J]. BMC Bioinformatics, 19
  • [36] scMAE: a masked autoencoder for single-cell RNA-seq clustering
    Fang, Zhaoyu
    Zheng, Ruiqing
    Li, Min
    [J]. BIOINFORMATICS, 2024, 40 (01)
  • [37] Single-cell RNA-seq clustering: datasets, models, and algorithms
    Peng, Lihong
    Tian, Xiongfei
    Tian, Geng
    Xu, Junlin
    Huang, Xin
    Weng, Yanbin
    Yang, Jialiang
    Zhou, Liqian
    [J]. RNA BIOLOGY, 2020, 17 (06) : 765 - 783
  • [38] Improving Single-Cell RNA-seq Clustering by Integrating Pathways
    Zhang, Chenxing
    Gao, Lin
    Wang, Bingbo
    Gao, Yong
    [J]. BRIEFINGS IN BIOINFORMATICS, 2021, 22 (06)
  • [39] scCAN: Clustering With Adaptive Neighbor-Based Imputation Method for Single-Cell RNA-Seq Data
    Dong, Shujie
    Liu, Yuansheng
    Gong, Yongshun
    Dong, Xiangjun
    Zeng, Xiangxiang
    [J]. IEEE-ACM TRANSACTIONS ON COMPUTATIONAL BIOLOGY AND BIOINFORMATICS, 2024, 21 (01) : 95 - 105
  • [40] Identification of cancer subtypes from single-cell RNA-seq data using a consensus clustering method
    Yanglan Gan
    Ning Li
    Guobing Zou
    Yongchang Xin
    Jihong Guan
    [J]. BMC Medical Genomics, 11