{"title":"A survey of biclustering and clustering methods in clustering different types of single-cell RNA sequencing data.","authors":"Chaowang Lan, Xiaoqi Tang, Caihua Liu","doi":"10.1093/bfgp/elaf010","DOIUrl":null,"url":null,"abstract":"<p><p>Single-cell RNA sequencing (scRNA-seq) technology has garnered considerable attention as it enables the exploration of cellular heterogeneity from a single-cell perspective. Various unsupervised methods, such as biclustering and clustering methods, offer a theoretical foundation for understanding the structure and function of cells. However, accurately identifying cell subtypes within complex scRNA-seq data remains challenging. To evaluate the current development status; summarize the strengths, weaknesses, and improvement strategies of unsupervised methods; and provide guidelines for future research, we surveyed five biclustering and 21 clustering methods applied to different types of scRNA-seq datasets. We employed three external and two internal metrics to determine clustering performance on 10 publicly available real datasets. Dataset properties are quantified from six perspectives to discover the most suitable biclustering or clustering methods. The results of this survey indicate that biclustering methods are effective for identifying local consistency or for deeply mining partially annotated datasets. Conversely, clustering methods are more suitable for dealing with unknown datasets. This survey aids in identifying cellular heterogeneity by recommending appropriate methods based on different dataset characteristics.</p>","PeriodicalId":55323,"journal":{"name":"Briefings in Functional Genomics","volume":"24 ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342763/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Briefings in Functional Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/bfgp/elaf010","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Single-cell RNA sequencing (scRNA-seq) technology has garnered considerable attention as it enables the exploration of cellular heterogeneity from a single-cell perspective. Various unsupervised methods, such as biclustering and clustering methods, offer a theoretical foundation for understanding the structure and function of cells. However, accurately identifying cell subtypes within complex scRNA-seq data remains challenging. To evaluate the current development status; summarize the strengths, weaknesses, and improvement strategies of unsupervised methods; and provide guidelines for future research, we surveyed five biclustering and 21 clustering methods applied to different types of scRNA-seq datasets. We employed three external and two internal metrics to determine clustering performance on 10 publicly available real datasets. Dataset properties are quantified from six perspectives to discover the most suitable biclustering or clustering methods. The results of this survey indicate that biclustering methods are effective for identifying local consistency or for deeply mining partially annotated datasets. Conversely, clustering methods are more suitable for dealing with unknown datasets. This survey aids in identifying cellular heterogeneity by recommending appropriate methods based on different dataset characteristics.
期刊介绍:
Briefings in Functional Genomics publishes high quality peer reviewed articles that focus on the use, development or exploitation of genomic approaches, and their application to all areas of biological research. As well as exploring thematic areas where these techniques and protocols are being used, articles review the impact that these approaches have had, or are likely to have, on their field. Subjects covered by the Journal include but are not restricted to: the identification and functional characterisation of coding and non-coding features in genomes, microarray technologies, gene expression profiling, next generation sequencing, pharmacogenomics, phenomics, SNP technologies, transgenic systems, mutation screens and genotyping. Articles range in scope and depth from the introductory level to specific details of protocols and analyses, encompassing bacterial, fungal, plant, animal and human data.
The editorial board welcome the submission of review articles for publication. Essential criteria for the publication of papers is that they do not contain primary data, and that they are high quality, clearly written review articles which provide a balanced, highly informative and up to date perspective to researchers in the field of functional genomics.