A new gene regulatory network reconstruction method based on single cell sequencing and transfer entropy

基因调控网络 计算机科学 传递熵 推论 熵(时间箭头) 构造(python库) 动态贝叶斯网络 数据挖掘 人工智能 基因 最大熵原理 生物 贝叶斯网络 基因表达 遗传学 量子力学 物理 程序设计语言
作者
Zhengtong Zhu,Jing Gao,Zhenyu Liu
标识
DOI:10.1117/12.2674758
摘要

In systems biology, gene regulatory networks can well reveal complex biological systems and dynamic biological processes. Traditional gene regulatory network reconstruction methods ignore dynamic biological processes. A gene regulatory network reconstruction method based on transfer entropy and single-cell dynamic time series data is proposed to solve this problem. And from a theoretical point of view, the possibility and rationality of transfer entropy in the application of big data and causal reasoning are proved in detail. Firstly, the method construct pseudo-time series dynamic gene expression data based on trajectory inference. Secondly, The transfer entropy is used to calculate the directional transfer information between paired genes, and screen the major gene regulatory relationships . Finally, remove the indirect gene regulation relationship according to the data processing inequality, and construct the gene regulation network . This method takes the single cell sequencing data of early mouse embryo blood development as an example, and selects TENET and DynGENIE3 algorithms as comparisons, which proves the feasibility and effectiveness of this method from the theoretical and experimental perspectives. The experimental results not only identify the key cell development regulatory factors and regulatory relationships, but also consume less time. It can not only provide important reference value and assumptions for biological disturbance experiment, but also reduce the time cost and research cost of biological experiment.
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