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DeGNServer:通过高性能逆向工程分析破译基因组规模的基因网络。

DeGNServer: deciphering genome-scale gene networks through high performance reverse engineering analysis.

作者信息

Li Jun, Wei Hairong, Zhao Patrick Xuechun

机构信息

Bioinformatics Lab, Plant Biology Division, Samuel Roberts Noble Foundation, 2510 Sam Noble Parkway, Ardmore, OK 73401, USA.

出版信息

Biomed Res Int. 2013;2013:856325. doi: 10.1155/2013/856325. Epub 2013 Nov 17.

DOI:10.1155/2013/856325
PMID:24328032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3847961/
Abstract

Analysis of genome-scale gene networks (GNs) using large-scale gene expression data provides unprecedented opportunities to uncover gene interactions and regulatory networks involved in various biological processes and developmental programs, leading to accelerated discovery of novel knowledge of various biological processes, pathways and systems. The widely used context likelihood of relatedness (CLR) method based on the mutual information (MI) for scoring the similarity of gene pairs is one of the accurate methods currently available for inferring GNs. However, the MI-based reverse engineering method can achieve satisfactory performance only when sample size exceeds one hundred. This in turn limits their applications for GN construction from expression data set with small sample size. We developed a high performance web server, DeGNServer, to reverse engineering and decipher genome-scale networks. It extended the CLR method by integration of different correlation methods that are suitable for analyzing data sets ranging from moderate to large scale such as expression profiles with tens to hundreds of microarray hybridizations, and implemented all analysis algorithms using parallel computing techniques to infer gene-gene association at extraordinary speed. In addition, we integrated the SNBuilder and GeNa algorithms for subnetwork extraction and functional module discovery. DeGNServer is publicly and freely available online.

摘要

利用大规模基因表达数据对基因组规模的基因网络(GNs)进行分析,为揭示参与各种生物过程和发育程序的基因相互作用及调控网络提供了前所未有的机会,从而加速了对各种生物过程、途径和系统新知识的发现。目前广泛使用的基于互信息(MI)对基因对相似性进行评分的相关性上下文似然度(CLR)方法,是目前可用于推断基因网络的准确方法之一。然而,基于互信息的逆向工程方法只有在样本量超过一百时才能取得令人满意的性能。这反过来限制了它们在从小样本量表达数据集中构建基因网络的应用。我们开发了一个高性能的网络服务器DeGNServer,用于逆向工程和解译基因组规模的网络。它通过整合不同的相关方法扩展了CLR方法,这些方法适用于分析从中等规模到大规模的数据集,如具有数十到数百次微阵列杂交的表达谱,并使用并行计算技术实现了所有分析算法,以极快的速度推断基因-基因关联。此外,我们整合了SNBuilder和GeNa算法用于子网提取和功能模块发现。DeGNServer可在网上公开免费获取。

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