Spectral clustering of single cells using Siamese nerual network combined with improved affinity matrix
Jiang, Hanjing2; Huang, Yabing3; Li, Qianpeng1
刊名BRIEFINGS IN BIOINFORMATICS
2022-04-13
页码12
关键词scRNA-seq Sigmoid kernel Siamese CNN improved spectral clustering
ISSN号1467-5463
DOI10.1093/bib/bbac113
通讯作者Huang, Yabing(ybhuangwhu@163.com)
英文摘要Limitations of bulk sequencing techniques on cell heterogeneity and diversity analysis have been pushed with the development of single-cell RNA-sequencing (scRNA-seq). To detect clusters of cells is a key step in the analysis of scRNA-seq. However, the high-dimensionality of scRNA-seq data and the imbalances in the number of different subcellular types are ubiquitous in real scRNA-seq data sets, which poses a huge challenge to the single-cell-type detection.We propose a meta-learning-based model, SiaClust, which is the combination of Siamese Convolutional Neural Network (CNN) and improved spectral clustering, to achieve scRNA-seq cell type detection. To be specific, with the help of the constrained Sigmoid kernel, the raw high-dimensionality data is mapped to a low-dimensional space, and the Siamese CNN learns the differences between the cell types in the low-dimensional feature space. The similarity matrix learned by Siamese CNN is used in combination with improved spectral clustering and t-distribution Stochastic Neighbor Embedding (t-SNE) for visualization. SiaClust highlights the differences between cell types by comparing the similarity of the samples, whereas blurring the differences within the cell types is better in processing high-dimensional and imbalanced data. SiaClust significantly improves clustering accuracy by using data generated by nine different species and tissues through different scNA-seq protocols for extensive evaluation, as well as analogies to state-of-the-art single-cell clustering models. More importantly, SiaClust accurately locates the exact site of dropout gene, and is more flexible with data size and cell type.
资助项目National Natural Science Foundation of China[62172171]
WOS关键词CELLULAR HETEROGENEITY ; GENE-EXPRESSION ; EMBRYOS ; FATE
WOS研究方向Biochemistry & Molecular Biology ; Mathematical & Computational Biology
语种英语
出版者OXFORD UNIV PRESS
WOS记录号WOS:000785718100001
资助机构National Natural Science Foundation of China
内容类型期刊论文
源URL[http://ir.ia.ac.cn/handle/173211/48304]  
专题国家专用集成电路设计工程技术研究中心_新型计算技术
通讯作者Huang, Yabing
作者单位1.Chinese Acad Sci, Inst Automat, Beijing, Peoples R China
2.Huazhong Univ Sci & Technol, Inst Artificial Intelligence, Key Lab Image Informat Proc & Intelligent Control, Sch Artificial Intelligence & Automat,Educ Minist, Wuhan 430074, Peoples R China
3.Wuhan Univ, Dept Pathol, Renmin Hosp, Wuhan 430060, Peoples R China
推荐引用方式
GB/T 7714
Jiang, Hanjing,Huang, Yabing,Li, Qianpeng. Spectral clustering of single cells using Siamese nerual network combined with improved affinity matrix[J]. BRIEFINGS IN BIOINFORMATICS,2022:12.
APA Jiang, Hanjing,Huang, Yabing,&Li, Qianpeng.(2022).Spectral clustering of single cells using Siamese nerual network combined with improved affinity matrix.BRIEFINGS IN BIOINFORMATICS,12.
MLA Jiang, Hanjing,et al."Spectral clustering of single cells using Siamese nerual network combined with improved affinity matrix".BRIEFINGS IN BIOINFORMATICS (2022):12.
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