Evidence map›Paper›PMID 40131310›Full record

ArticleBriefings in bioinformatics2025

scSAMAC: saliency-adjusted masking induced attention contrastive learning for single-cell clustering.

Bo Li, Yongkang Zhao, Jing Hu, Shihua Zhang, Xiaolong Zhang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Bo LiSchool of Computer Science and Technology, Wuhan University of Science and Technology, Huangjiahu west road 2#, Wuhan 430065, China.ORCID 0000-0003-1009-7195
Yongkang ZhaoSchool of Computer Science and Technology, Wuhan University of Science and Technology, Huangjiahu west road 2#, Wuhan 430065, China.
Jing HuSchool of Computer Science and Technology, Wuhan University of Science and Technology, Huangjiahu west road 2#, Wuhan 430065, China.ORCID 0000-0003-1348-8773
Shihua ZhangCollege of Computer Science, South-Central Minzu University, 182# Minyuan road, Hongshan District, Wuhan 430074, China.
Xiaolong ZhangSchool of Computer Science and Technology, Wuhan University of Science and Technology, Huangjiahu west road 2#, Wuhan 430065, China.

Funding

National Natural Science Foundation of China 61972299
6 · The paper itself

Abstract

Single-cell sequencing technology has enabled researchers to study cellular heterogeneity at the cell level. To facilitate the downstream analysis, clustering single-cell data into subgroups is essential. However, the high dimensionality, sparsity, and dropout events of the data make the clustering challenging. Currently, many deep learning methods have been proposed. Nevertheless, they either fail to fully utilize pairwise distances information between similar cells, or do not adequately capture their feature correlations. They cannot also effectively handle high-dimensional sparse data. Therefore, they are not suitable for high-fidelity clustering, leading to difficulties in analyzing the clear cell types required for downstream analysis. The proposed scSAMAC method integrates contrastive learning and negative binomial losses into a variational autoencoder, extracting features via contrastive unit similarity while preserving the intrinsic characteristics. This enhances the robustness and generalization during the clustering. In the contrastive learning, it constructs a mask module by adopting a negative sample generation method with gene feature saliency adjustment, which selects features more influential in the clustering phase and simulates data missing events. Additionally, it develops a novel loss, which consists of a soft k-means loss, a Wasserstein distance, and a contrastive loss. This fully utilizes data information and improves clustering performance. Furthermore, a multi-head attention mechanism module is applied to the latent variables at each layer of autoencoder to enhance feature correlation, integration, and information repair. Experimental results demonstrate that scSAMAC outperforms several state-of-the-art clustering methods.

Indexed as

Computational BiologyDeep LearningSingle-Cell AnalysisAlgorithmsCluster AnalysisHumansclusteringcontrastive learningfeaturessingle cells

Identifiers

PMID40131310
PMCPMC11934584

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.