BootCellNet 是一种基于重采样的程序,它通过对基因调控网络的稳健推断,促进对细胞群的无监督识别。

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2024-09-30 eCollection Date: 2024-09-01 DOI:10.1371/journal.pcbi.1012480
Yutaro Kumagai
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引用次数: 0

摘要

测量技术,尤其是单细胞 RNA 测序(scRNA-seq)技术的最新进展,彻底改变了我们获取大量细胞状态全息数据的能力。随着测量技术的发展,对数据分析方法的需求也越来越大,特别是那些专注于细胞类型鉴定和基因调控网络(GRN)推断的方法。我们开发了一种名为 "BootCellNet "的新方法,利用平滑和重采样来推断基因调控网络。利用推断出的 GRN,BootCellNet 进一步推断出最小优势集(MDS),这是一组决定整个网络动态的基因。我们已经证明,BootCellNet 能从 scRNA-seq 数据中稳健地推断出 GRNs 及其 MDSs,并能利用外周血单核细胞和造血的 scRNA-seq 数据集促进细胞集群的无监督识别。它还识别了 COVID-19 患者特异性细胞及其潜在的调控转录因子。BootCellNet 不仅能以无监督和可解释的方式识别细胞类型,还能通过推断 GRN 和 MDS 深入了解已识别细胞类型的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BootCellNet, a resampling-based procedure, promotes unsupervised identification of cell populations via robust inference of gene regulatory networks.

Recent advances in measurement technologies, particularly single-cell RNA sequencing (scRNA-seq), have revolutionized our ability to acquire large amounts of omics-level data on cellular states. As measurement techniques evolve, there has been an increasing need for data analysis methodologies, especially those focused on cell-type identification and inference of gene regulatory networks (GRNs). We have developed a new method named BootCellNet, which employs smoothing and resampling to infer GRNs. Using the inferred GRNs, BootCellNet further infers the minimum dominating set (MDS), a set of genes that determines the dynamics of the entire network. We have demonstrated that BootCellNet robustly infers GRNs and their MDSs from scRNA-seq data and facilitates unsupervised identification of cell clusters using scRNA-seq datasets of peripheral blood mononuclear cells and hematopoiesis. It has also identified COVID-19 patient-specific cells and their potential regulatory transcription factors. BootCellNet not only identifies cell types in an unsupervised and explainable way but also provides insights into the characteristics of identified cell types through the inference of GRNs and MDS.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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