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首页> 外文期刊>Journal of Bioinformatics and Computational Biology >RANKING DIFFERENTIAL HUBS IN GENE CO-EXPRESSION NETWORKS
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RANKING DIFFERENTIAL HUBS IN GENE CO-EXPRESSION NETWORKS

机译:基因共表达网络中排名差分集线器

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Identifying the genes that change their expressions between two conditions (such as normal versus cancer) is a crucial task that can help in understanding the causes of diseases. Differential networking has emerged as a powerful approach to detect the changes in network structures and to identify the differentially connected genes among two networks. However, existing differential network-based methods primarily depend on pairwise comparisons of the genes based on their connectivity. Therefore, these methods cannot capture the essential topological changes in the network structures. In this paper, we propose a novel algorithm, DiffRank, which ranks the genes based on their contribution to the differences between the two networks. To achieve this goal, we define two novel structural scoring measures: a local structure measure (differential connectivity) and a global structure measure (differential betweenness centrality). These measures are optimized by propagating the scores through the network structure and then ranking the genes based on these propagated scores. We demonstrate the effectiveness of DiffRank on synthetic and real datasets. For the synthetic datasets, we developed a simulator for generating synthetic differential scale-free networks, and we compared our method with existing methods. The comparisons show that our algorithm outperforms these existing methods. For the real datasets, we apply the proposed algorithm on several gene expression datasets and demonstrate that the proposed method provides biologically interesting results.
机译:鉴定改变其两个条件(例如正常癌症)之间表达的基因是一个重要任务,可以帮助理解疾病的原因。差分网络已成为检测网络结构的变化的强大方法,并识别两个网络中的差分连接基因。然而,基于差分网络的方法主要取决于基因的成对比较基于它们的连接。因此,这些方法无法捕获网络结构中的基本拓扑变化。在本文中,我们提出了一种新颖的算法,Diffrank,基于它们对两个网络之间的差异进行贡献。为实现这一目标,我们定义了两种新颖的结构评分措施:局部结构措施(差分连接)和全球结构测量(差分间中心之间)。通过通过网络结构传播得分,然后基于这些传播的分数对基因进行排序来进行优化这些措施。我们展示了Siffrank对合成和实时数据集的有效性。对于合成数据集,我们开发了一种用于产生合成差分尺度网络的模拟器,并将我们的方法与现有方法进行了比较。比较显示我们的算法优于这些现有方法。对于真实数据集,我们在几个基因表达数据集上应用所提出的算法,并证明所提出的方法提供生物学上有趣的结果。

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