Structure-guided feature and cluster contrastive learning for multi-view clustering

Multi-view clustering (MVC) technology performs unsupervised clustering on data collected from multiple sources, and has received intense attention in recent years. However, most existing MVC methods fail to consider retaining view-specific information when learning multi-view consistent representat...

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Veröffentlicht in:Neurocomputing (Amsterdam) 2024-05, Vol.582, p.127555, Article 127555
Hauptverfasser: Shu, Zhenqiu, Li, Bin, Mao, Cunli, Gao, Shengxiang, Yu, Zhengtao
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Sprache:eng
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Zusammenfassung:Multi-view clustering (MVC) technology performs unsupervised clustering on data collected from multiple sources, and has received intense attention in recent years. However, most existing MVC methods fail to consider retaining view-specific information when learning multi-view consistent representations. Besides, the feature and cluster structures of multi-view data cannot be fully leveraged in clustering. In this paper, we propose a structure-guided feature and cluster contrastive learning (SGFCC) for multi-view clustering. Specifically, SGFCC utilizes autoencoders to achieve view-specific information reconstruction in feature space, and extracts high-level features for multi-view consistent representation learning to eliminate the effects of view-specific information and noise on consistent representation. To fully capture the similar clustering structure of high-level features and semantic features of samples across different views, we adopt a structure-guided feature-level and cluster-level contrastive learning strategy in our SGFCC model. Furthermore, we design a clustering layer to explore the cluster structure of high-level features. Different from most existing MVC methods, our method applies a non-fusion scheme that aggregates the semantic information of all views to obtain the final semantic labels. Extensive experiments on public datasets demonstrate that our method outperforms other competitors in clustering tasks.
ISSN:0925-2312
1872-8286
DOI:10.1016/j.neucom.2024.127555