Time-coexpress: temporal trajectory modeling of dynamic gene co-expression patterns using single-cell transcriptomics data.

IF 3.3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Shuyi Yang, Anderson Bussing, Giampiero Marra, Michelle L Brinkmeier, Sally A Camper, Shannon W Davis, Yen-Yi Ho
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引用次数: 0

Abstract

Background: The rapid advancement of single-cell RNA sequencing (scRNAseq) technology provides high-resolution views of transcriptomic activity within individual cells. Most routine analyses of scRNAseq data focus on individual genes; however, the one-gene-at-a-time analysis is likely to miss meaningful genetic interactions. Gene co-expression analysis addresses this limitation by identifying coordinated changes in gene expression in response to cellular conditions, such as developmental or temporal trajectories. Existing approaches to gene co-expression analysis often assume restrictive linear relationships. However, gene co-expression can change in complex, non-linear ways, which suggests the need for more flexible and accurate methods.

Results: We propose a copula-based framework, TIME-CoExpress, with proper data-driven smoothing functions to model non-linear changes in gene co-expression along cellular temporal trajectories. Our method provides the flexibility to incorporate characteristics commonly observed in scRNAseq data, such as over-dispersion and zero-inflation, into the modeling framework. In addition to modeling gene co-expression, TIME-CoExpress captures dynamic changes in gene-level zero-inflation rates and mean expression levels, providing a more comprehensive analysis of scRNAseq data. Through a series of simulation analyses, we evaluated the performance of the proposed approach. We further demonstrated its implementation using a scRNAseq dataset and identified differentially co-expressed gene pairs along the cellular temporal trajectory during pituitary embryonic development, comparing [Formula: see text] and wild-type mice.

Conclusions: The proposed framework enables flexible and robust identification of dynamic, non-linear changes in gene co-expression, zero-inflation rates, and mean expression levels along temporal trajectories in scRNAseq data. Detecting these changes provides deeper insights into the biological processes and offers a better understanding of gene regulation throughout cellular development.

时间共表达:利用单细胞转录组学数据建立动态基因共表达模式的时间轨迹模型。
背景:快速发展的单细胞RNA测序(scRNAseq)技术提供了单个细胞内转录组活性的高分辨率视图。大多数scnaseq数据的常规分析都集中在单个基因上;然而,一次一个基因的分析可能会错过有意义的基因相互作用。基因共表达分析通过识别响应细胞条件(如发育或时间轨迹)的基因表达的协调变化来解决这一限制。现有的基因共表达分析方法通常假设有限制的线性关系。然而,基因共表达可以以复杂的非线性方式改变,这表明需要更灵活和准确的方法。结果:我们提出了一个基于copula的框架TIME-CoExpress,它具有适当的数据驱动平滑函数来模拟基因共表达沿细胞时间轨迹的非线性变化。我们的方法提供了将scRNAseq数据中常见的特征(如过度分散和零膨胀)合并到建模框架中的灵活性。除了对基因共表达进行建模外,TIME-CoExpress还捕获了基因水平零膨胀率和平均表达水平的动态变化,为scRNAseq数据提供了更全面的分析。通过一系列的仿真分析,我们评估了该方法的性能。我们使用scRNAseq数据集进一步证明了其实现,并在垂体胚胎发育过程中沿细胞时间轨迹确定了差异共表达的基因对,并将[公式:见文本]与野生型小鼠进行比较。结论:所提出的框架能够灵活而稳健地识别scnaseq数据中基因共表达、零膨胀率和平均表达水平沿时间轨迹的动态、非线性变化。检测这些变化可以更深入地了解生物过程,并更好地了解细胞发育过程中的基因调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Bioinformatics
BMC Bioinformatics 生物-生化研究方法
CiteScore
5.70
自引率
3.30%
发文量
506
审稿时长
4.3 months
期刊介绍: BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology. BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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