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Protein functional module identification method combining topological features and gene expression data

机译:蛋白质功能模块识别方法结合拓扑特征和基因表达数据

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摘要

More and more clustering algorithms are proposed to identify protein complexes with the constantly development of proteomics. Although many of those algorithms have been verified to have good performance [1–4], mining the complex only through the protein network itself will inevitably limit the effectiveness of its results, because the available protein data is incomplete due to the diversity of protein network structures and the complexity of data sources, and there is a certain amount of noise in protein networks. Therefore, other biological data such as fusion of gene expression provide new ideas for detecting protein functional modules [5, 6]. For example, Chin et al. [7] proposed method HUNTER to detect functional modules, this method firstly calculates the similarity value of high-throughput data (for example, calculating pairwise similarity of gene expression patterns from microarray data), then, detecting weak signals that cannot be distinguished with existing methods by using the network of genes or proteins and the similarity values between them and by applying network topological constraints to the expression data clusters, finding connected sub-networks (or modules) with highly similarity, which improves the effectiveness of compound identification. Although there are many ways to analyze the network and similar data separately [8–11], there is still a lot of room for development in the method of using two information sources for analysis.
机译:提出了越来越多的聚类算法以识别蛋白质组学的不断发展的蛋白质复合物。虽然已经验证了许多算法以具有良好的性能[1-4],但仅通过蛋白质网络本身开采复合体将不可避免地限制其结果的有效性,因为由于蛋白质网络的多样性,可用的蛋白质数据是不完整的结构和数据源的复杂性,蛋白质网络中存在一定程度的噪音。因此,其他生物数据如融合的基因表达,为检测蛋白质功能模块进行了新的思路[5,6]。例如,Chin等人。 [7]提出的方法猎人检测功能模块,该方法首先计算高吞吐量数据的相似性值(例如,从微阵列数据计算基因表达式模式的成对相似性),然后检测无法与现有的弱信号方法通过使用基因网络或蛋白质网络以及它们之间的相似性值以及将网络拓扑限制应用于表达数据集群,以高度相似地找到连接的子网(或模块),从而提高了化合物识别的有效性。虽然有很多方法可以单独分析网络和类似数据[8-11],但是在使用两个信息源进行分析的方法中仍有大量的开发空间。

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