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Quasi-bicliques: Complexity and Binding Pairs

机译:准双bicliques:复杂性和绑定对

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摘要

Protein-protein interactions (PPIs) are one of the most important mechanisms in cellular processes. To model protein interaction sites, recent studies have suggested to find interacting protein group pairs from large PPI networks at the first step, and then to search conserved motifs within the protein groups to form interacting motif pairs. To consider noise effect and incompleteness of biological data, we propose to use quasi-bicliques for finding interacting protein group pairs. We investigate two new problems which arise from finding interacting protein group pairs: the maximum vertex quasi-biclique problem and the maximum balanced quasi-biclique problem. We prove that both problems are NP-hard. This is a surprising result as the widely known maximum vertex biclique problem is polynomial time solvable [16]. We then propose a heuristic algorithm which uses the greedy method to find the quasi-bicliques from PPI networks. Our experiment results on real data show that this algorithm has a better performance than a benchmark algorithm for identifying highly matched BLOCKS and PRINTS motifs.
机译:蛋白质-蛋白质相互作用(PPI)是细胞过程中最重要的机制之一。为了对蛋白质相互作用位点进行建模,最近的研究建议首先从大型PPI网络中找到相互作用的蛋白质组对,然后在蛋白质组内搜索保守的基序以形成相互作用的基序对。考虑到噪声效应和生物学数据的不完整性,我们建议使用准双斜体来查找相互作用的蛋白质组对。我们调查了发现相互作用的蛋白质组对而产生的两个新问题:最大顶点拟双斜向问题和最大平衡拟双斜向问题。我们证明这两个问题都是NP难题。这是一个令人惊讶的结果,因为众所周知的最大顶点双斜边问题是多项式时间可解的[16]。然后,我们提出了一种启发式算法,该算法使用贪婪方法从PPI网络中找到准双三次方。我们在真实数据上的实验结果表明,该算法在识别高度匹配的BLOCKS和PRINTS图案方面比基准算法具有更好的性能。

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