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首页> 外文期刊>Briefings in bioinformatics >Integrative approaches for predicting protein function and prioritizing genes for complex phenotypes using protein interaction networks
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Integrative approaches for predicting protein function and prioritizing genes for complex phenotypes using protein interaction networks

机译:使用蛋白质相互作用网络预测蛋白质功能并确定复杂表型基因优先级的整合方法

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With the rapid development of biotechnologies, many types of biological data includingmolecular networks are now available. However, to obtain a more complete understanding of a biological system, the integration of molecular networks with other data, such as molecular sequences, protein domains and gene expression profiles, is needed. A key to the use of networks in biological studies is the definition of similarity among proteins over the networks. Here, we review applications of similarity measures over networks with a special focus on the following four problems: (i) predicting protein functions, (ii) prioritizing genes related to a phenotype given a set of seed genes that have been shown to be related to the phenotype, (iii) prioritizing genes related to a phenotype by integrating gene expression profiles and networks and (iv) identification of false positives and false negatives from RNAi experiments. Diffusion kernels are demonstrated to give superior performance in all these tasks, leading to the suggestion that diffusion kernels should be the primary choice for a network similarity metric over other similarity measures such as direct neighbors and shortest path distance.
机译:随着生物技术的飞速发展,包括分子网络在内的许多类型的生物数据现在都可以得到。但是,为了更全面地了解生物系统,需要将分子网络与其他数据(例如分子序列,蛋白质结构域和基因表达谱)进行整合。在生物学研究中使用网络的关键是定义网络中蛋白质之间的相似性。在这里,我们回顾了网络上相似性度量的应用,特别关注以下四个问题:(i)预测蛋白质功能,(ii)优先考虑与表型相关的基因,并给出一组已证明与之相关的种子基因表型,(iii)通过整合基因表达谱和网络对与表型相关的基因进行优先排序,以及(iv)从RNAi实验中识别假阳性和假阴性。事实证明,扩散内核在所有这些任务中均具有出色的性能,这表明,与其他相似性度量标准(例如直接邻居和最短路径距离)相比,扩散内核应是网络相似性度量标准的主要选择。

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