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Genetic network inference: from co-expression clustering to reverse engineering.

机译:遗传网络推论:从共表达聚类到逆向工程。

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MOTIVATION: Advances in molecular biological, analytical and computational technologies are enabling us to systematically investigate the complex molecular processes underlying biological systems. In particular, using high-throughput gene expression assays, we are able to measure the output of the gene regulatory network. We aim here to review datamining and modeling approaches for conceptualizing and unraveling the functional relationships implicit in these datasets. Clustering of co-expression profiles allows us to infer shared regulatory inputs and functional pathways. We discuss various aspects of clustering, ranging from distance measures to clustering algorithms and multiple-cluster memberships. More advanced analysis aims to infer causal connections between genes directly, i.e. who is regulating whom and how. We discuss several approaches to the problem of reverse engineering of genetic networks, from discrete Boolean networks, to continuous linear and non-linear models. We conclude that the combination of predictive modeling with systematic experimental verification will be required to gain a deeper insight into living organisms, therapeutic targeting and bioengineering.
机译:动机:分子生物学,分析和计算技术的进步使我们能够系统地研究生物学系统下的复杂分子过程。特别是,使用高通量基因表达测定,我们能够测量基因调控网络的输出。我们的目的是在这里回顾数据挖掘和建模方法,以概念化和揭示这些数据集中隐含的功能关系。共表达谱的聚类使我们能够推断出共享的监管投入和功能途径。我们讨论了聚类的各个方面,从距离度量到聚类算法和多聚类成员资格。更高级的分析旨在直接推断基因之间的因果关系,即谁在调节谁以及如何调节。我们讨论了遗传网络逆向工程问题的几种方法,从离散布尔网络到连续线性和非线性模型。我们得出结论,将需要将预测模型与系统的实验验证相结合,以更深入地了解活生物体,靶向治疗和生物工程。

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