ST-SCSR: identifying spatial domains in spatial transcriptomics data via structure correlation and self-representation.

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Briefings in bioinformatics Pub Date : 2024-07-25 DOI:10.1093/bib/bbae437
Min Zhang, Wensheng Zhang, Xiaoke Ma
{"title":"ST-SCSR: identifying spatial domains in spatial transcriptomics data via structure correlation and self-representation.","authors":"Min Zhang, Wensheng Zhang, Xiaoke Ma","doi":"10.1093/bib/bbae437","DOIUrl":null,"url":null,"abstract":"<p><p>Recent advances in spatial transcriptomics (ST) enable measurements of transcriptome within intact biological tissues by preserving spatial information, offering biologists unprecedented opportunities to comprehensively understand tissue micro-environment, where spatial domains are basic units of tissues. Although great efforts are devoted to this issue, they still have many shortcomings, such as ignoring local information and relations of spatial domains, requiring alternatives to solve these problems. Here, a novel algorithm for spatial domain identification in Spatial Transcriptomics data with Structure Correlation and Self-Representation (ST-SCSR), which integrates local information, global information, and similarity of spatial domains. Specifically, ST-SCSR utilzes matrix tri-factorization to simultaneously decompose expression profiles and spatial network of spots, where expressional and spatial features of spots are fused via the shared factor matrix that interpreted as similarity of spatial domains. Furthermore, ST-SCSR learns affinity graph of spots by manipulating expressional and spatial features, where local preservation and sparse constraints are employed, thereby enhancing the quality of graph. The experimental results demonstrate that ST-SCSR not only outperforms state-of-the-art algorithms in terms of accuracy, but also identifies many potential interesting patterns.</p>","PeriodicalId":9209,"journal":{"name":"Briefings in bioinformatics","volume":null,"pages":null},"PeriodicalIF":6.8000,"publicationDate":"2024-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11372132/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Briefings in bioinformatics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/bib/bbae437","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

Recent advances in spatial transcriptomics (ST) enable measurements of transcriptome within intact biological tissues by preserving spatial information, offering biologists unprecedented opportunities to comprehensively understand tissue micro-environment, where spatial domains are basic units of tissues. Although great efforts are devoted to this issue, they still have many shortcomings, such as ignoring local information and relations of spatial domains, requiring alternatives to solve these problems. Here, a novel algorithm for spatial domain identification in Spatial Transcriptomics data with Structure Correlation and Self-Representation (ST-SCSR), which integrates local information, global information, and similarity of spatial domains. Specifically, ST-SCSR utilzes matrix tri-factorization to simultaneously decompose expression profiles and spatial network of spots, where expressional and spatial features of spots are fused via the shared factor matrix that interpreted as similarity of spatial domains. Furthermore, ST-SCSR learns affinity graph of spots by manipulating expressional and spatial features, where local preservation and sparse constraints are employed, thereby enhancing the quality of graph. The experimental results demonstrate that ST-SCSR not only outperforms state-of-the-art algorithms in terms of accuracy, but also identifies many potential interesting patterns.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ST-SCSR:通过结构相关性和自我呈现识别空间转录组学数据中的空间域。
空间转录组学(ST)的最新进展通过保留空间信息实现了对完整生物组织内转录组的测量,为生物学家全面了解组织微环境提供了前所未有的机会,而空间域是组织的基本单位。尽管人们在这一问题上付出了巨大努力,但它们仍然存在许多缺陷,如忽略了空间域的局部信息和关系,需要其他方法来解决这些问题。本文提出了一种利用结构相关性和自我呈现(ST-SCSR)在空间转录组学数据中识别空间域的新算法,该算法综合了空间域的局部信息、全局信息和相似性。具体来说,ST-SCSR 利用矩阵三因子化(matrix tri-factorization)同时分解表达谱和斑点的空间网络,通过共享因子矩阵融合斑点的表达和空间特征,从而解释为空间域的相似性。此外,ST-SCSR 还通过处理表达和空间特征来学习斑点的亲和图,其中采用了局部保留和稀疏约束,从而提高了图的质量。实验结果表明,ST-SCSR 不仅在准确性方面优于最先进的算法,而且还能识别出许多潜在的有趣模式。
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 去求助
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.
期刊最新文献
TUnA: an uncertainty-aware transformer model for sequence-based protein-protein interaction prediction. scLEGA: an attention-based deep clustering method with a tendency for low expression of genes on single-cell RNA-seq data. CatLearning: highly accurate gene expression prediction from histone mark. Detecting novel cell type in single-cell chromatin accessibility data via open-set domain adaptation. Explorer: efficient DNA coding by De Bruijn graph toward arbitrary local and global biochemical constraints.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1