{"title":"Tuning hyperparameters of doublet-detection methods for single-cell RNA sequencing data.","authors":"Nan Miles Xi, Angelos Vasilopoulos","doi":"10.15302/J-QB-022-0324","DOIUrl":null,"url":null,"abstract":"<p><p>Doublet is a major confounder in single-cell RNA sequencing data analysis. Computational doublet-detection methods aim to remove doublets from scRNA-seq data. The performance of those methods relies on the appropriate setting of their hyperparameters. In this study, we explore the optimal hyperparameters for scDblFinder, a cutting-edge doublet-detection method. Our optimization utilizes a full factorial design, a response surface model, and 16 real scRNA-seq datasets. The optimal hyperparameters achieve top doublet-detection performance under a wide range of biological conditions. Our methodology is applicable to broader computational methods in scRNA-seq data analysis.</p><p><strong>Background: </strong>The existence of doublets in single-cell RNA sequencing (scRNA-seq) data poses a great challenge in downstream data analysis. Computational doublet-detection methods have been developed to remove doublets from scRNA-seq data. Yet, the default hyperparameter settings of those methods may not provide optimal performance.</p><p><strong>Methods: </strong>We propose a strategy to tune hyperparameters for a cutting-edge doublet-detection method. We utilize a full factorial design to explore the relationship between hyperparameters and detection accuracy on 16 real scRNA-seq datasets. The optimal hyperparameters are obtained by a response surface model and convex optimization.</p><p><strong>Results: </strong>We show that the optimal hyperparameters provide top performance across scRNA-seq datasets under various biological conditions. Our tuning strategy can be applied to other computational doublet-detection methods. It also offers insights into hyperparameter tuning for broader computational methods in scRNA-seq data analysis.</p><p><strong>Conclusions: </strong>The hyperparameter configuration significantly impacts the performance of computational doublet-detection methods. Our study is the first attempt to systematically explore the optimal hyperparameters under various biological conditions and optimization objectives. Our study provides much-needed guidance for hyperparameter tuning in computational doublet-detection methods.</p>","PeriodicalId":45660,"journal":{"name":"Quantitative Biology","volume":"1 1","pages":"297-305"},"PeriodicalIF":1.4000,"publicationDate":"2023-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12807224/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Quantitative Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.15302/J-QB-022-0324","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/9/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Doublet is a major confounder in single-cell RNA sequencing data analysis. Computational doublet-detection methods aim to remove doublets from scRNA-seq data. The performance of those methods relies on the appropriate setting of their hyperparameters. In this study, we explore the optimal hyperparameters for scDblFinder, a cutting-edge doublet-detection method. Our optimization utilizes a full factorial design, a response surface model, and 16 real scRNA-seq datasets. The optimal hyperparameters achieve top doublet-detection performance under a wide range of biological conditions. Our methodology is applicable to broader computational methods in scRNA-seq data analysis.
Background: The existence of doublets in single-cell RNA sequencing (scRNA-seq) data poses a great challenge in downstream data analysis. Computational doublet-detection methods have been developed to remove doublets from scRNA-seq data. Yet, the default hyperparameter settings of those methods may not provide optimal performance.
Methods: We propose a strategy to tune hyperparameters for a cutting-edge doublet-detection method. We utilize a full factorial design to explore the relationship between hyperparameters and detection accuracy on 16 real scRNA-seq datasets. The optimal hyperparameters are obtained by a response surface model and convex optimization.
Results: We show that the optimal hyperparameters provide top performance across scRNA-seq datasets under various biological conditions. Our tuning strategy can be applied to other computational doublet-detection methods. It also offers insights into hyperparameter tuning for broader computational methods in scRNA-seq data analysis.
Conclusions: The hyperparameter configuration significantly impacts the performance of computational doublet-detection methods. Our study is the first attempt to systematically explore the optimal hyperparameters under various biological conditions and optimization objectives. Our study provides much-needed guidance for hyperparameter tuning in computational doublet-detection methods.
期刊介绍:
Quantitative Biology is an interdisciplinary journal that focuses on original research that uses quantitative approaches and technologies to analyze and integrate biological systems, construct and model engineered life systems, and gain a deeper understanding of the life sciences. It aims to provide a platform for not only the analysis but also the integration and construction of biological systems. It is a quarterly journal seeking to provide an inter- and multi-disciplinary forum for a broad blend of peer-reviewed academic papers in order to promote rapid communication and exchange between scientists in the East and the West. The content of Quantitative Biology will mainly focus on the two broad and related areas: ·bioinformatics and computational biology, which focuses on dealing with information technologies and computational methodologies that can efficiently and accurately manipulate –omics data and transform molecular information into biological knowledge. ·systems and synthetic biology, which focuses on complex interactions in biological systems and the emergent functional properties, and on the design and construction of new biological functions and systems. Its goal is to reflect the significant advances made in quantitatively investigating and modeling both natural and engineered life systems at the molecular and higher levels. The journal particularly encourages original papers that link novel theory with cutting-edge experiments, especially in the newly emerging and multi-disciplinary areas of research. The journal also welcomes high-quality reviews and perspective articles.