deCS:人体组织中单细胞RNA测序数据的系统细胞类型注释工具

Guangsheng Pei, F. Yan, L. Simon, Yulin Dai, P. Jia, Zhongming Zhao
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引用次数: 12

摘要

单细胞RNA测序(scRNA-seq)正在彻底改变复杂和动态细胞机制的研究。然而,细胞类型注释仍然是一个主要的挑战,因为它很大程度上依赖于先验知识和人工管理,这是繁琐和不准确的。越来越多的scRNA-seq数据集,以及大量已发表的遗传研究,促使我们建立一个全面的人类细胞类型参考图谱。在这里,我们提出了deCS(解码细胞类型特异性),这是一种通过全面收集人类细胞类型表达谱和标记基因来增强的自动细胞类型注释方法。我们使用deCS对来自不同组织类型的scRNA-seq数据进行标注,并系统评估了不同条件下的标注准确性,包括参考面板、测序深度和特征选择策略。我们的研究结果表明,扩展引用对于提高标注准确性至关重要。与许多现有的最先进的注释工具相比,deCS显著减少了计算时间并提高了准确性。deCS可以集成到标准的scRNA-seq分析管道中,以增强细胞类型注释。最后,我们展示了deCS在51个人类复杂性状中鉴定性状-细胞类型关联的广泛效用,为疾病发病的细胞机制提供了更深入的见解。所有文档,包括源代码、用户手册、演示数据和教程,都可以在https://github.com/bsml320/deCS上免费获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
deCS: A Tool for Systematic Cell Type Annotations of Single-cell RNA Sequencing Data among Human Tissues
Single-cell RNA sequencing (scRNA-seq) is revolutionizing the study of complex and dynamic cellular mechanisms. However, cell-type annotation remains a main challenge as it largely relies on a priori knowledge and manual curation, which is cumbersome and less accurate. The increasing number of scRNA-seq data sets, as well as numerous published genetic studies, motivated us to build a comprehensive human cell type reference atlas. Here, we present deCS (decoding Cell type-Specificity), an automatic cell type annotation method augmented by a comprehensive collection of human cell type expression profiles and marker genes. We used deCS to annotate scRNA-seq data from various tissue types and systematically evaluated the annotation accuracy under different conditions, including reference panels, sequencing depth and feature selection strategies. Our results demonstrated that expanding the references is critical for improving annotation accuracy. Compared to many existing state-of-the-art annotation tools, deCS significantly reduced computation time and increased accuracy. deCS can be integrated into the standard scRNA-seq analytical pipeline to enhance cell type annotation. Finally, we demonstrated the broad utility of deCS to identify trait-cell type associations in 51 human complex traits, providing deeper insights into the cellular mechanisms of disease pathogenesis. All documents, including source code, user manual, demo data, and tutorials, are freely available at https://github.com/bsml320/deCS.
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