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Reverse engineering biomolecular systems using -omic data: Challenges, progress and opportunities

机译:使用组学数据逆向工程生物分子系统:挑战,进展和机遇

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摘要

Recent advances in high-throughput biotechnologies have led to the rapid growing research interest in reverse engineering of biomolecular systems (REBMS). 'Data-driven' approaches, i.e. data mining, can be used to extract patterns from large volumes of biochemical data at molecular-level resolution while 'design-driven' approaches, i.e. systems modeling, can be used to simulate emergent system properties. Consequently, both data- and design-driven approaches applied to -omic data may lead to novel insights in reverse engineering biological systems that could not be expected before using low-throughput platforms. However, there exist several challenges in this fast growing field of reverse engineering biomolecular systems: (i) to integrate heterogeneous biochemical data for data mining, (ii) to combine top-down and bottom-up approaches for systems modeling and (iii) to validate system models experimentally. In addition to reviewing progress made by the community and opportunities encountered in addressing these challenges, we explore the emerging field of synthetic biology, which is an exciting approach to validate and analyze theoretical system models directly through experimental synthesis, i.e. analysis-by-synthesis. The ultimate goal is to address the present and future challenges in reverse engineering biomolecular systems (REBMS) using integrated workflow of data mining, systems modeling and synthetic biology.
机译:高通量生物技术的最新进展导致对生物分子系统逆向工程(REBMS)的研究兴趣迅速增长。 ``数据驱动''的方法(即数据挖掘)可用于以分子水平的分辨率从大量生化数据中提取模式,而``设计驱动''的方法(即系统建模)可用于模拟紧急系统特性。因此,应用于组学数据的数据驱动方法和设计驱动方法都可以在逆向工程生物系统中带来新颖的见解,而这在使用低通量平台之前是无法期望的。但是,在反向工程生物分子系统这个快速发展的领域中存在一些挑战:(i)整合异构生化数据以进行数据挖掘;(ii)结合自上而下和自下而上的方法进行系统建模;以及(iii)通过实验验证系统模型。除了回顾社区取得的进展以及在应对这些挑战方面遇到的机遇外,我们还将探索合成生物学的新兴领域,这是一种令人兴奋的方法,可以直接通过实验合成(即合成分析)来验证和分析理论系统模型。最终目标是使用数据挖掘,系统建模和合成生物学的集成工作流程来应对逆向工程生物分子系统(REBMS)的当前和未来挑战。

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