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鉴定浆细胞游离转录组起源的组织或细胞类型方法的综合评估。

Comprehensive evaluation of methods for identifying tissues or cell types of origin of the plasma cell-free transcriptome.

作者信息

Yang Tingyu, Qin Yulong, Yan Shuo, Guo Sijia, Sun Jinghua, Huang Jiayi, Li Jiayi, Zhou Qing, Jin Xin, Wang Wen-Jing

机构信息

College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.

BGI Research, Shenzhen, China.

出版信息

PeerJ. 2025 Apr 17;13:e19241. doi: 10.7717/peerj.19241. eCollection 2025.

Abstract

Plasma cell-free RNA (cfRNA) is derived from cells in various tissues and organs throughout the body and reflects the physiological and pathological conditions. Identifying the origins of cfRNA is essential for comprehending its variations. Only a few tools are designed for cfRNA deconvolution, and most studies have relied on traditional bulk RNA methods. In this study, we employed human tissue and cell transcriptomic data as reference sets and evaluated the performance of seven deconvolution methods on cfRNA. We compared the analysis results of cell types and tissues of origin of plasma cfRNA and chose to use single-cell RNA sequencing (scRNA-seq) data as reference to conduct further evaluation of deconvolution methods. Subsequently, we assessed the accuracy and robustness of the methods by utilizing simulated cfRNA data generated from scRNA-seq. We also evaluated the methods' accuracy on real plasma cfRNA data by analyzing the correlation between the predicted cell proportions and the corresponding clinical indicators. Moreover, we compared the methods' effectiveness in revealing the impacts of diseases on cells and evaluated the performance of cancer classification models based on the cell origin data they provided. In summary, our study provides valuable insights into cfRNA origin analysis, enhancing its potential in biomedical research.

摘要

血浆游离RNA(cfRNA)源自全身各种组织和器官中的细胞,反映生理和病理状况。识别cfRNA的来源对于理解其变异至关重要。仅设计了少数几种用于cfRNA反卷积的工具,并且大多数研究依赖于传统的批量RNA方法。在本研究中,我们将人类组织和细胞转录组数据用作参考集,并评估了七种反卷积方法对cfRNA的性能。我们比较了血浆cfRNA的细胞类型和来源组织的分析结果,并选择使用单细胞RNA测序(scRNA-seq)数据作为参考,对反卷积方法进行进一步评估。随后,我们通过利用从scRNA-seq生成的模拟cfRNA数据来评估这些方法的准确性和稳健性。我们还通过分析预测的细胞比例与相应临床指标之间的相关性,评估了这些方法对真实血浆cfRNA数据的准确性。此外,我们比较了这些方法在揭示疾病对细胞影响方面的有效性,并基于它们提供的细胞起源数据评估了癌症分类模型的性能。总之,我们的研究为cfRNA起源分析提供了有价值的见解,增强了其在生物医学研究中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dcc/12009560/8755fd263382/peerj-13-19241-g001.jpg

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