scSFCL:Deep clustering of scRNA-seq data with subspace feature confidence learning

IF 2.6 4区 生物学 Q2 BIOLOGY Computational Biology and Chemistry Pub Date : 2024-11-22 DOI:10.1016/j.compbiolchem.2024.108292
Xiaokun Meng, Yuanyuan Zhang, Xiaoyu Xu, Kaihao Zhang, Baoming Feng
{"title":"scSFCL:Deep clustering of scRNA-seq data with subspace feature confidence learning","authors":"Xiaokun Meng,&nbsp;Yuanyuan Zhang,&nbsp;Xiaoyu Xu,&nbsp;Kaihao Zhang,&nbsp;Baoming Feng","doi":"10.1016/j.compbiolchem.2024.108292","DOIUrl":null,"url":null,"abstract":"<div><div>The rapid development of single-cell RNA sequencing(scRNA-seq) technology has spawned a variety of single-cell clustering methods. These methods combine statistics and bioinformatics to reveal differences in gene expression between cells and the diversity of cell types. Deep exploration of single-cell data is more challenging due to the high dimensionality, sparsity and noise of scRNA-seq data. Discriminative attribute information is often difficult to be fully utilised, while traditional clustering methods may not accurately capture the diversity of cell types. Therefore, a deep clustering method is proposed for scRNA-seq data based on subspace feature confidence learning called scSFCL. By dividing the subspace based on kernel density, discriminative feature subsets are filtered. The feature confidence of the subset is learned by combining the graph convolutional network (GCN) with weighting. Also, scSFCL facilitates the complementary fusion of generic structural and idiosyncratic information through a mutually supervised clustering that integrates GCN and a denoising variational autoencoder based on zero-inflated negative binomials (DVAE-ZINB). By validation on multiple scRNA-seq datasets, it is shown that the clustering performance of scSFCL is significantly improved compared with traditional methods, providing an effective solution for deep clustering of scRNA-seq data.</div></div>","PeriodicalId":10616,"journal":{"name":"Computational Biology and Chemistry","volume":"114 ","pages":"Article 108292"},"PeriodicalIF":2.6000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computational Biology and Chemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1476927124002809","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The rapid development of single-cell RNA sequencing(scRNA-seq) technology has spawned a variety of single-cell clustering methods. These methods combine statistics and bioinformatics to reveal differences in gene expression between cells and the diversity of cell types. Deep exploration of single-cell data is more challenging due to the high dimensionality, sparsity and noise of scRNA-seq data. Discriminative attribute information is often difficult to be fully utilised, while traditional clustering methods may not accurately capture the diversity of cell types. Therefore, a deep clustering method is proposed for scRNA-seq data based on subspace feature confidence learning called scSFCL. By dividing the subspace based on kernel density, discriminative feature subsets are filtered. The feature confidence of the subset is learned by combining the graph convolutional network (GCN) with weighting. Also, scSFCL facilitates the complementary fusion of generic structural and idiosyncratic information through a mutually supervised clustering that integrates GCN and a denoising variational autoencoder based on zero-inflated negative binomials (DVAE-ZINB). By validation on multiple scRNA-seq datasets, it is shown that the clustering performance of scSFCL is significantly improved compared with traditional methods, providing an effective solution for deep clustering of scRNA-seq data.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
scSFCL:利用子空间特征置信度学习对 scRNA-seq 数据进行深度聚类
单细胞 RNA 测序(scRNA-seq)技术的快速发展催生了多种单细胞聚类方法。这些方法将统计学和生物信息学相结合,揭示了细胞间基因表达的差异和细胞类型的多样性。由于 scRNA-seq 数据的高维性、稀疏性和噪声,单细胞数据的深度探索更具挑战性。判别属性信息往往难以充分利用,而传统的聚类方法可能无法准确捕捉细胞类型的多样性。因此,我们提出了一种基于子空间特征置信度学习的 scRNA-seq 数据深度聚类方法,称为 scSFCL。通过基于核密度划分子空间,筛选出具有区分度的特征子集。子集的特征置信度是通过结合带权重的图卷积网络(GCN)来学习的。此外,scSFCL 还通过整合 GCN 和基于零膨胀负二项式(DVAE-ZINB)的去噪变异自动编码器的相互监督聚类,促进了通用结构信息和特异性信息的互补融合。通过在多个 scRNA-seq 数据集上的验证表明,与传统方法相比,scSFCL 的聚类性能显著提高,为 scRNA-seq 数据的深度聚类提供了有效的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Computational Biology and Chemistry
Computational Biology and Chemistry 生物-计算机:跨学科应用
CiteScore
6.10
自引率
3.20%
发文量
142
审稿时长
24 days
期刊介绍: Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered. Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered. Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.
期刊最新文献
scSFCL:Deep clustering of scRNA-seq data with subspace feature confidence learning A structure-based approach to discover a potential isomerase Pin1 inhibitor for cancer therapy using computational simulation and biological studies A multi-perspective deep learning framework for enhancer characterization and identification Vector embeddings by sequence similarity and context for improved compression, similarity search, clustering, organization, and manipulation of cDNA libraries MuSE: A deep learning model based on multi-feature fusion for super-enhancer prediction
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1