scAGCI: an anchor graph-based method for cell clustering from integrated scRNA-seq and scATAC-seq data.

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Yao Dong, Jiaxue Zhang, Jin Shi, Yushan Hu, Xiaowen Cao, Yongfeng Dong, Xuekui Zhang
{"title":"scAGCI: an anchor graph-based method for cell clustering from integrated scRNA-seq and scATAC-seq data.","authors":"Yao Dong, Jiaxue Zhang, Jin Shi, Yushan Hu, Xiaowen Cao, Yongfeng Dong, Xuekui Zhang","doi":"10.1093/bib/bbaf244","DOIUrl":null,"url":null,"abstract":"<p><p>Single-cell multi-omics clustering confronts noise and heterogeneity barriers. Current multi-view anchor graph approaches, though successful in noise reduction, inadequately model higher order feature interactions. To address this issue, we propose scAGCI, a cell clustering method based on anchor graphs that integrates both scRNA-seq and scATAC-seq data. Our method captures specific and shared anchor graphs representing the properties of omics data in the process of dynamic anchor unification, and mines high-order shared information to complete the omics representation. Subsequently, clustering results are obtained by integrating the specific and shared omics representation. Benchmarking against 13 state-of-the-art methods confirms scAGCI's superior clustering performance and computational efficiency in cell-type identification and subtype resolution. The method preserves biologically meaningful omics patterns, as evidenced by marker gene enrichment and functional analyses, establishing it as a robust tool for elucidating cellular heterogeneity in single-cell multi-omics data.</p>","PeriodicalId":9209,"journal":{"name":"Briefings in bioinformatics","volume":"26 4","pages":""},"PeriodicalIF":6.8000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12232420/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Briefings in bioinformatics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/bib/bbaf244","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Single-cell multi-omics clustering confronts noise and heterogeneity barriers. Current multi-view anchor graph approaches, though successful in noise reduction, inadequately model higher order feature interactions. To address this issue, we propose scAGCI, a cell clustering method based on anchor graphs that integrates both scRNA-seq and scATAC-seq data. Our method captures specific and shared anchor graphs representing the properties of omics data in the process of dynamic anchor unification, and mines high-order shared information to complete the omics representation. Subsequently, clustering results are obtained by integrating the specific and shared omics representation. Benchmarking against 13 state-of-the-art methods confirms scAGCI's superior clustering performance and computational efficiency in cell-type identification and subtype resolution. The method preserves biologically meaningful omics patterns, as evidenced by marker gene enrichment and functional analyses, establishing it as a robust tool for elucidating cellular heterogeneity in single-cell multi-omics data.

scAGCI:一种基于锚点图的方法,从集成的scRNA-seq和scATAC-seq数据中进行细胞聚类。
单细胞多组学聚类面临噪声和异质性障碍。目前的多视图锚图方法虽然在降噪方面取得了成功,但对高阶特征相互作用的建模不足。为了解决这个问题,我们提出了scAGCI,这是一种基于锚点图的细胞聚类方法,它集成了scRNA-seq和scATAC-seq数据。该方法在动态锚点统一过程中捕获代表组学数据属性的特定锚点图和共享锚点图,并挖掘高阶共享信息来完成组学表示。随后,通过整合特定组学表示和共享组学表示得到聚类结果。对13种最先进的方法进行基准测试,证实了scAGCI在细胞类型识别和亚型分辨率方面的卓越聚类性能和计算效率。正如标记基因富集和功能分析所证明的那样,该方法保留了生物学上有意义的组学模式,使其成为阐明单细胞多组学数据中细胞异质性的强大工具。
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 求助全文
来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信