Storm: Incorporating transient stochastic dynamics to infer the RNA velocity with metabolic labeling information.

IF 3.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Qiangwei Peng, Xiaojie Qiu, Tiejun Li
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引用次数: 0

Abstract

The time-resolved scRNA-seq (tscRNA-seq) provides the possibility to infer physically meaningful kinetic parameters, e.g., the transcription, splicing or RNA degradation rate constants with correct magnitudes, and RNA velocities by incorporating temporal information. Previous approaches utilizing the deterministic dynamics and steady-state assumption on gene expression states are insufficient to achieve favorable results for the data involving transient process. We present a dynamical approach, Storm (Stochastic models of RNA metabolic-labeling), to overcome these limitations by solving stochastic differential equations of gene expression dynamics. The derivation reveals that the new mRNA sequencing data obeys different types of cell-specific Poisson distributions when jointly considering both biological and cell-specific technical noise. Storm deals with measured counts data directly and extends the RNA velocity methodology based on metabolic labeling scRNA-seq data to transient stochastic systems. Furthermore, we relax the constant parameter assumption over genes/cells to obtain gene-cell-specific transcription/splicing rates and gene-specific degradation rates, thus revealing time-dependent and cell-state-specific transcriptional regulations. Storm will facilitate the study of the statistical properties of tscRNA-seq data, eventually advancing our understanding of the dynamic transcription regulation during development and disease.

风暴结合瞬态随机动力学,利用代谢标记信息推断 RNA 的速度。
时间分辨 scRNA-seq(tscRNA-seq)为推断有物理意义的动力学参数提供了可能,例如,转录、剪接或 RNA 降解速率常数的正确幅度,以及通过结合时间信息推断 RNA 速度。以往利用确定性动力学和基因表达状态稳态假设的方法不足以为涉及瞬时过程的数据取得有利结果。我们提出了一种名为 Storm(RNA 代谢标记随机模型)的动态方法,通过求解基因表达动态的随机微分方程来克服这些限制。推导结果表明,当同时考虑生物噪声和细胞特异性技术噪声时,新的 mRNA 测序数据服从不同类型的细胞特异性泊松分布。Storm 直接处理测量的计数数据,并将基于代谢标记 scRNA-seq 数据的 RNA 速度方法扩展到瞬态随机系统。此外,我们放宽了对基因/细胞的恒定参数假设,以获得基因细胞特异性转录/剪接率和基因特异性降解率,从而揭示了时间依赖性和细胞状态特异性转录调控。Storm 将有助于研究 tscRNA-seq 数据的统计特性,最终促进我们对发育和疾病过程中动态转录调控的理解。
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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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