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AI 根据所提供的论文材料归类:摘要研究生物动态调控网络和 ODE 建模,未直接讨论所列微观网络、干扰或结构经济模型。

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代码、数据与补充材料

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关注这篇论文的作者
Tao Lu
Hua Liang
Hongzhe Li
Hulin Wu

结合混合效应建模的高维常微分方程动态基因调控网络识别

研究问题
高维基因系统存在正负调控及反馈作用,如何在降低维度的同时识别动态调控关系,并构建模块间的有向网络?
方法与思路
作者将 ODE、聚类降维与混合效应建模结合,提出 CSIEF 五步流程,使用非参数平滑、SCAD 选择和 SAEM 参数估计。
材料陈述的贡献
摘要称流程可量化模块间调控与反馈,对关键 SCAD 选择步骤提供渐近分析及模拟验证,并应用于酵母细胞周期数据。
阅读关注点
应核对聚类与平滑误差如何影响后续网络估计、ODE 参数的可辨识性,以及 SCAD 理论条件、反馈解释和功能富集依据。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明;摘要只明确关键选择步骤的理论验证,不能推断完整流程均有保证或网络关系已获因果确认。

原文摘要

Gene regulation is a complicated process. The interaction of many genes and their products forms an intricate biological network. Identification of this dynamic network will help us understand the biological process in a systematic way. However, the construction of such a dynamic network is very challenging for a high-dimensional system. In this article we propose to use a set of ordinary differential equations (ODE), coupled with dimensional reduction by clustering and mixed-effects modeling techniques, to model the dynamic gene regulatory network (GRN). The ODE models allow us to quantify both positive and negative gene regulations as well as feedback effects of one set of genes in a functional module on the dynamic expression changes of the genes in another functional module, which results in a directed graph network. A five-step procedure, Clustering, Smoothing, regulation Identification, parameter Estimates refining and Function enrichment analysis (CSIEF) is developed to identify the ODE-based dynamic GRN. In the proposed CSIEF procedure, a series of cutting-edge statistical methods and techniques are employed, that include non-parametric mixed-effects models with a mixture distribution for clustering, nonparametric mixed-effects smoothing-based methods for ODE models, the smoothly clipped absolute deviation (SCAD)-based variable selection, and stochastic approximation EM (SAEM) approach for mixed-effects ODE model parameter estimation. The key step, the SCAD-based variable selection of the proposed procedure is justified by investigating its asymptotic properties and validated by Monte Carlo simulations. We apply the proposed method to identify the dynamic GRN for yeast cell cycle progression data. We are able to annotate the identified modules through function enrichment analyses. Some interesting biological findings are discussed. The proposed procedure is a promising tool for constructing a general dynamic GRN and more complicated dynamic networks.

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