{"title":"transCAE:利用迁移学习和卷积自编码器增强单细胞RNA-seq数据的细胞类型注释。","authors":"Qingchun Liu, Yan Xu","doi":"10.1016/j.jmb.2025.168936","DOIUrl":null,"url":null,"abstract":"<div><div>Single-cell RNA sequencing (scRNA-seq) analysis offers tremendous potential for addressing various biological questions, with one key application being the annotation of query datasets with unknown cell types using well-annotated external reference datasets. However, the performance of existing supervised or semi-supervised methods largely depends on the quality of source data. Furthermore, these methods often struggle with the batch effects arising from different platforms when handling multiple reference or query datasets, making precise annotation challenging. We developed transCAE, a robust transfer learning-based algorithm for single-cell annotation that integrates unsupervised dimensionality reduction with supervised cell type classification. This approach fully leverages information from both reference and query datasets to achieve precise cell classification within the query data. Extensive evaluations show that transCAE significantly enhances classification accuracy and efficiently mitigates batch effects. Compared to other state-of-the-art methods, transCAE demonstrates superior performance in experiments involving multiple reference or query datasets. These strengths position transCAE as an optimal annotation method for scRNA-seq datasets.</div></div>","PeriodicalId":369,"journal":{"name":"Journal of Molecular Biology","volume":"437 4","pages":"Article 168936"},"PeriodicalIF":4.7000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"transCAE: Enhancing Cell Type Annotation in Single-cell RNA-seq Data with Transfer Learning and Convolutional Autoencoder\",\"authors\":\"Qingchun Liu, Yan Xu\",\"doi\":\"10.1016/j.jmb.2025.168936\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Single-cell RNA sequencing (scRNA-seq) analysis offers tremendous potential for addressing various biological questions, with one key application being the annotation of query datasets with unknown cell types using well-annotated external reference datasets. However, the performance of existing supervised or semi-supervised methods largely depends on the quality of source data. Furthermore, these methods often struggle with the batch effects arising from different platforms when handling multiple reference or query datasets, making precise annotation challenging. We developed transCAE, a robust transfer learning-based algorithm for single-cell annotation that integrates unsupervised dimensionality reduction with supervised cell type classification. This approach fully leverages information from both reference and query datasets to achieve precise cell classification within the query data. Extensive evaluations show that transCAE significantly enhances classification accuracy and efficiently mitigates batch effects. Compared to other state-of-the-art methods, transCAE demonstrates superior performance in experiments involving multiple reference or query datasets. These strengths position transCAE as an optimal annotation method for scRNA-seq datasets.</div></div>\",\"PeriodicalId\":369,\"journal\":{\"name\":\"Journal of Molecular Biology\",\"volume\":\"437 4\",\"pages\":\"Article 168936\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-01-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022283625000026\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022283625000026","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
transCAE: Enhancing Cell Type Annotation in Single-cell RNA-seq Data with Transfer Learning and Convolutional Autoencoder
Single-cell RNA sequencing (scRNA-seq) analysis offers tremendous potential for addressing various biological questions, with one key application being the annotation of query datasets with unknown cell types using well-annotated external reference datasets. However, the performance of existing supervised or semi-supervised methods largely depends on the quality of source data. Furthermore, these methods often struggle with the batch effects arising from different platforms when handling multiple reference or query datasets, making precise annotation challenging. We developed transCAE, a robust transfer learning-based algorithm for single-cell annotation that integrates unsupervised dimensionality reduction with supervised cell type classification. This approach fully leverages information from both reference and query datasets to achieve precise cell classification within the query data. Extensive evaluations show that transCAE significantly enhances classification accuracy and efficiently mitigates batch effects. Compared to other state-of-the-art methods, transCAE demonstrates superior performance in experiments involving multiple reference or query datasets. These strengths position transCAE as an optimal annotation method for scRNA-seq datasets.
期刊介绍:
Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions.
Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.