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Systematic construction of gene coexpression networks with applications to human T helper cell differentiation process

机译:基因共表达网络的系统构建及其在人类T辅助细胞分化过程中的应用

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摘要

Motivation: Coexpression networks have recently emerged as a novel holistic approach to microarray data analysis and interpretation. Choosing an appropriate cutoff threshold, above which a gene-gene interaction is considered as relevant, is a critical task in most network-centric applications, especially when two or more networks are being compared. Results: We demonstrate that the performance of traditional approaches, which are based on a pre-defined cutoff or significance level, can vary drastically depending on the type of data and application. Therefore, we introduce a systematic procedure for estimating a cutoff threshold of coexpression networks directly from their topological properties. Both synthetic and real datasets show clear benefits of our data-driven approach under various practical circumstances. In particular, the procedure provides a robust estimate of individual degree distributions, even from multiple microarray studies performed with different array platforms or experimental designs, which can be used to discriminate the corresponding phenotypes. Application to human T helper cell differentiation process provides useful insights into the components and interactions controlling this process, many of which would have remained unidentified on the basis of expression change alone. Moreover, several human-mouse orthologs showed conserved topological changes in both systems, suggesting their potential importance in the differentiation process. Contact: laliel@utu.fi Supplementary information: Supplementary data are available at Bioinformatics online.
机译:动机:共表达网络最近作为微阵列数据分析和解释的一种新颖的整体方法而出现。在大多数以网络为中心的应用中,尤其是在比较两个或多个网络时,选择一个适当的临界阈值是一项至关重要的任务,在该阈值之上,基因与基因的相互作用被认为是相关的。结果:我们证明,基于预定义的临界值或显着性水平的传统方法的性能可能会因数据类型和应用程序而异。因此,我们引入了一种系统的程序,可直接从它们的拓扑属性估计共表达网络的截止阈值。在各种实际情况下,综合数据集和实际数据集都显示出我们的数据驱动方法的明显好处。尤其是,该程序甚至可以从使用不同阵列平台或实验设计进行的多个微阵列研究中,也可以对各个学位分布进行可靠的估计,这些研究可用于区分相应的表型。在人类T辅助细胞分化过程中的应用为控制该过程的组件和相互作用提供了有用的见识,其中许多仅凭表达变化仍无法确定。此外,几种人鼠直系同源物在两个系统中均显示出保守的拓扑变化,表明它们在分化过程中的潜在重要性。联系人:laliel@utu.fi补充信息:补充数据可从在线生物信息学获得。

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