Analysis of time-series regulatory networks

被引:7
|
作者
Ding, Jun [1 ]
Bar-Joseph, Ziv [1 ]
机构
[1] Carnegie Mellon Univ, Computat Biol Dept, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
Time series; Regulatory networks; Dynamic biological processes; RNA-SEQ; DIFFERENTIATION; DYNAMICS; IDENTIFICATION; DISCOVERY; INFERENCE; GENOME; GENES;
D O I
10.1016/j.coisb.2020.07.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The vast majority of biological processes are dynamic, changing over time. Several studies profile high-throughput time-series data and use it for analyzing and modeling various biological processes. In this review, we focus on data, methods, and analysis for reconstructing dynamic regulatory network models from high-throughput time-series data sets. We discuss methods focused on a single data type, methods that integrate several omics data types, methods that integrate static and time-series data, and methods that focus on single-cell data. For each of these categories, we present some of the top methods and discuss their underlying assumptions, advantages, and potential shortcomings. As the quantity and types of time-series omics data continue to increase, we expect that these methods, and additional methods extending and improving them, would play an increasingly important role in our ability to accurately model biological processes.
引用
收藏
页码:16 / 24
页数:9
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