TY - GEN
T1 - Label-Guided Graph Contrastive Learning for Single-Cell Fusion Clustering
AU - Qin, Baojuan
AU - Shang, Junliang
AU - Zhao, Yan
AU - Zhang, Xiaohan
AU - Li, Feng
AU - Liu, Jin Xing
N1 - Publisher Copyright:
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2026.
PY - 2026
Y1 - 2026
N2 - Single-cell RNA sequencing (scRNA-seq) technology provides gene expression information at the individual cell level and reveals cellular heterogeneity within tissues. Cell clustering is an important task in scRNA-seq data analysis. Although many single-cell clustering methods have been proposed, existing methods often fail to fully consider both cell attribute information and the structural relationships between cells. Moreover, many graph clustering methods combine with contrastive learning, but most graph contrastive learning methods overlook the similarity between nodes. To address this, a label-guided graph contrastive learning-based single-cell fusion clustering method, scLGGCL, is proposed. First, a dual-reconstruction information fusion module is constructed to extract both the latent attribute information and the relationships between cells, thus obtaining a fusion of attribute and structural information. Next, a label-guided graph contrastive learning module is designed to capture semantic-level feature similarity between nodes and adjust the distance between positive and negative nodes based on predicted label information. Finally, a deep embedding clustering-based self-optimization module is introduced, which utilizes the fused attribute and structural information to optimize the clustering results and pull cells toward the cluster centers. The validity and accuracy of scLGGCL clustering were verified by comparing with other single-cell clustering methods on both single datasets and cross-datasets. The source code of scLGGCL is available at https://github.com/CDMBlab/scLGGCL.
AB - Single-cell RNA sequencing (scRNA-seq) technology provides gene expression information at the individual cell level and reveals cellular heterogeneity within tissues. Cell clustering is an important task in scRNA-seq data analysis. Although many single-cell clustering methods have been proposed, existing methods often fail to fully consider both cell attribute information and the structural relationships between cells. Moreover, many graph clustering methods combine with contrastive learning, but most graph contrastive learning methods overlook the similarity between nodes. To address this, a label-guided graph contrastive learning-based single-cell fusion clustering method, scLGGCL, is proposed. First, a dual-reconstruction information fusion module is constructed to extract both the latent attribute information and the relationships between cells, thus obtaining a fusion of attribute and structural information. Next, a label-guided graph contrastive learning module is designed to capture semantic-level feature similarity between nodes and adjust the distance between positive and negative nodes based on predicted label information. Finally, a deep embedding clustering-based self-optimization module is introduced, which utilizes the fused attribute and structural information to optimize the clustering results and pull cells toward the cluster centers. The validity and accuracy of scLGGCL clustering were verified by comparing with other single-cell clustering methods on both single datasets and cross-datasets. The source code of scLGGCL is available at https://github.com/CDMBlab/scLGGCL.
KW - Clustering analysis
KW - Graph contrastive learning
KW - Information fusion
KW - Label-guided
KW - Single-cell RNA sequencing
UR - https://www.scopus.com/pages/publications/105013311100
U2 - 10.1007/978-981-95-0698-9_31
DO - 10.1007/978-981-95-0698-9_31
M3 - 会议稿件
AN - SCOPUS:105013311100
SN - 9789819506972
T3 - Lecture Notes in Computer Science
SP - 373
EP - 384
BT - Bioinformatics Research and Applications - 21st International Symposium, ISBRA 2025, Proceedings
A2 - Tang, Jing
A2 - Lai, Xin
A2 - Cai, Zhipeng
A2 - Peng, Wei
A2 - Wei, Yanjie
PB - Springer Science and Business Media Deutschland GmbH
T2 - 21st International Symposium on Bioinformatics Research and Applications, ISBRA 2025
Y2 - 3 August 2025 through 5 August 2025
ER -