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Novel Ranking Methods Applied to Complex Membership Determination Problems

机译:新颖的排序方法应用于复杂的成员资格确定问题

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The biological motivated problem that we want to solve in this paper is to predict the new members of a partially known protein complex (i.e. complex membership determination). In this problem, we are given a core set of proteins (i.e. the queries) making up a protein complex. However, the biologist experts do not know whether this core set is complete or not. Our objective is to find more potential members of the protein complex by ranking proteins in protein-protein interaction network. One of the solutions to this problem is a network reliability based method. Due to high time complexity of this method, the random walk on graphs method has been proposed to solve this complex membership determination problem. However, the random walk on graphs method is not the current state of the art network-based method solving bioinformatics problem. In this paper, the novel un-normalized graph (p-) Laplacian based ranking method will be developed based on the un-normalized graph p-Laplacian operator definitions such as the curvature operator of graph (i.e. the un-normalized graph 1-Laplacian operator) and will be used to solve the complex membership determination problem. The results from experiments shows that the un-normalized graph p-Laplacian ranking methods are at least as good as the current state of the art network-based ranking method (p=2) but often lead to better ranking accuracy performance measures.
机译:我们在本文中要解决的生物学动机问题是预测部分已知的蛋白质复合物的新成员(即复合物成员确定)。在这个问题中,我们得到了构成蛋白质复合物的一组核心蛋白质(即查询)。但是,生物学家专家不知道此核心集是否完整。我们的目标是通过在蛋白质-蛋白质相互作用网络中对蛋白质进行排名来找到蛋白质复合物的更多潜在成员。解决此问题的方法之一是基于网络可靠性的方法。由于该方法时间复杂度高,因此提出了随机行走图方法来解决该复杂的隶属度确定问题。然而,图上的随机游走方法不是解决生物信息学问题的基于网络的现有技术的当前状态。在本文中,将基于非标准化图p-Laplacian算子定义(例如图的曲率算子(即非标准化图1-Laplacian)运算符),并将用于解决复杂的成员资格确定问题。实验结果表明,未归一化的图p-Laplacian排名方法至少与当前基于网络的最先进排名方法(p = 2)一样好,但通常会导致更好的排名准确性性能指标。

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