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Differential dependency network analysis to identify condition-specific topological changes in biological networks

机译:差分依赖网络分析以识别生物网络中特定条件的拓扑变化

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摘要

>Motivation: Significant efforts have been made to acquire data under different conditions and to construct static networks that can explain various gene regulation mechanisms. However, gene regulatory networks are dynamic and condition-specific; under different conditions, networks exhibit different regulation patterns accompanied by different transcriptional network topologies. Thus, an investigation on the topological changes in transcriptional networks can facilitate the understanding of cell development or provide novel insights into the pathophysiology of certain diseases, and help identify the key genetic players that could serve as biomarkers or drug targets.>Results: Here, we report a differential dependency network (DDN) analysis to detect statistically significant topological changes in the transcriptional networks between two biological conditions. We propose a local dependency model to represent the local structures of a network by a set of conditional probabilities. We develop an efficient learning algorithm to learn the local dependency model using the Lasso technique. A permutation test is subsequently performed to estimate the statistical significance of each learned local structure. In testing on a simulation dataset, the proposed algorithm accurately detected all the genes with network topological changes. The method was then applied to the estrogen-dependent T-47D estrogen receptor-positive (ER+) breast cancer cell line datasets and human and mouse embryonic stem cell datasets. In both experiments using real microarray datasets, the proposed method produced biologically meaningful results. We expect DDN to emerge as an important bioinformatics tool in transcriptional network analyses. While we focus specifically on transcriptional networks, the DDN method we introduce here is generally applicable to other biological networks with similar characteristics.>Availability: The DDN MATLAB toolbox and experiment data are available at .>Contact: >Supplementary information: are available at Bioinformatics online.
机译:>动机:已经做出了巨大的努力来获取不同条件下的数据并构建可以解释各种基因调控机制的静态网络。然而,基因调控网络是动态的并且是条件特定的。在不同条件下,网络表现出不同的调控模式,并伴随着不同的转录网络拓扑。因此,对转录网络拓扑变化的研究可以促进对细胞发育的了解或对某些疾病的病理生理学提供新颖的见解,并有助于确定可用作生物标志物或药物靶标的关键遗传因素。>结果: 在这里,我们报告了差异依赖性网络(DDN)分析,以检测两种生物学条件之间转录网络中统计学上显着的拓扑变化。我们提出了局部依赖模型,以一组条件概率表示网络的局部结构。我们开发了一种有效的学习算法,以使用套索技术学习局部依赖模型。随后执行置换测试以估计每个学习的局部结构的统计显着性。在模拟数据集上进行测试时,所提出的算法可以准确地检测出具有网络拓扑变化的所有基因。然后将该方法应用于依赖雌激素的T-47D雌激素受体阳性(ER +)乳腺癌细胞系数据集以及人和小鼠胚胎干细胞数据集。在使用真实微阵列数据集的两个实验中,提出的方法均产生了生物学上有意义的结果。我们期望DDN在转录网络分析中成为重要的生物信息学工具。虽然我们专门关注转录网络,但是我们在此处介绍的DDN方法通常适用于具有类似特征的其他生物网络。>可用性: DDN MATLAB工具箱和实验数据可在以下网址获得。>联系方式: >补充信息:可在线访问生物信息学。

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