大规模单细胞rna测序数据的差分细胞通讯推断框架。

IF 2.8 Q1 GENETICS & HEREDITY
NAR Genomics and Bioinformatics Pub Date : 2025-06-19 eCollection Date: 2025-06-01 DOI:10.1093/nargab/lqaf084
Giulia Cesaro, Giacomo Baruzzo, Gaia Tussardi, Barbara Di Camillo
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引用次数: 0

摘要

单细胞转录组学数据已被广泛用于表征生物系统,特别是研究在许多生物过程中起重要作用的细胞-细胞通讯。尽管有各种计算工具可用于推断细胞通信,但在细胞间和细胞内水平上量化不同实验条件下的变化仍然具有挑战性。此外,可用的方法通常在分析不同实验设计的灵活性和以易于解释的方式可视化结果的能力方面受到限制。在这里,我们提出了一个可推广的计算框架,旨在从大规模单细胞转录组学数据推断和支持两种实验条件下的差异细胞通信分析。scSeqCommDiff工具采用基于统计和网络的计算方法,以快速和内存高效的方式表征改变的细胞串扰。该框架与CClens相辅相成,CClens是一个用户友好的Shiny应用程序,用于促进推断细胞-细胞通信的交互式分析。通过空间转录组学数据、与其他工具的比较以及大规模数据集(包括细胞图谱)的应用验证了该框架的可靠性、可扩展性和效率。此外,对单核转录组学数据集的应用显示了所提出的工作流程支持和揭示肌萎缩性侧索硬化症患者和健康受试者之间细胞-细胞相互作用变化的有效性和能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Differential cellular communication inference framework for large-scale single-cell RNA-sequencing data.

Differential cellular communication inference framework for large-scale single-cell RNA-sequencing data.

Differential cellular communication inference framework for large-scale single-cell RNA-sequencing data.

Differential cellular communication inference framework for large-scale single-cell RNA-sequencing data.

Single-cell transcriptomics data have been widely used to characterize biological systems, particularly in studying cell-cell communication, which plays a significant role in many biological processes. Despite the availability of various computational tools for inferring cellular communication, quantifying variations across different experimental conditions at both intercellular and intracellular levels remains challenging. Moreover, available methods are in general limited in terms of flexibility in analyzing different experimental designs and the ability to visualize results in an easily interpretable way. Here, we present a generalizable computational framework designed to infer and support differential cellular communication analysis across two experimental conditions from large-scale single-cell transcriptomics data. The scSeqCommDiff tool employs a statistical and network-based computational approach for characterizing altered cellular cross-talk in a fast and memory-efficient way. The framework is complemented with CClens, a user-friendly Shiny app to facilitate interactive analysis of inferred cell-cell communication. Validation through spatial transcriptomics data, comparison with other tools, and application to large-scale datasets (including a cell atlas) confirms the reliability, scalability, and efficiency of the framework. Moreover, the application to a single-nucleus transcriptomics dataset shows the validity and ability of the proposed workflow to support and unravel alterations in cell-cell interactions among patients with amyotrophic lateral sclerosis and healthy subjects.

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来源期刊
CiteScore
8.00
自引率
2.20%
发文量
95
审稿时长
15 weeks
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