A Heuristic Algorithm for Detecting Intercellular Interactions

Fahim Mohammad, R. Flight, Benjamin J. Harrison, J. Petruska, E. Rouchka
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Abstract

Existing analytical tools enable broad-scale experimentation ("-omics") to provide a great deal of information about intracellular processes. However, extraction of information regarding intercellular interactions, particularly from separate datasets, is generally more limited, principally for lack of specialized analytical tools. In turn, few experiments are designed to examine intercellular interactions. Using the large number of previously identified interactions available in databases may provide a useful platform for analyzing these interactions. However, finding all possible interactions is a computationally intensive task and quickly becomes intractable using a naive approach on networks with hundreds of thousands of nodes and edges. A heuristic algorithm similar to the "Backtracking algorithm" is proposed to find all possible protein interactions across any two gene sets. The algorithm starts with an initial set of genes and incrementally adds a candidate to the interaction network and abandons each candidate x as soon as it is determined that x does not lead to a valid solution. An exclusion vector (EV) is used to accomplish this task and is populated at each step, maintaining a list of those nodes that need to be excluded from interactions in the future and thus restricting the size of the network. The EV also allows location awareness by using Gene Ontology (GO) cell component classifications to discard nodes that are not relevant for the network. This algorithm can be readily applied to pathway analysis and the determination of elements underlying intercellular interactions.
一种检测细胞间相互作用的启发式算法
现有的分析工具使大规模的实验(“组学”)能够提供大量关于细胞内过程的信息。然而,关于细胞间相互作用的信息提取,特别是从单独的数据集中,通常是比较有限的,主要是因为缺乏专门的分析工具。反过来,很少有实验被设计用来检查细胞间的相互作用。使用数据库中大量先前确定的可用交互可以为分析这些交互提供一个有用的平台。然而,找到所有可能的交互是一项计算密集型任务,并且在具有数十万个节点和边的网络上使用朴素的方法很快变得难以处理。提出了一种类似于“回溯算法”的启发式算法来发现任意两个基因集之间所有可能的蛋白质相互作用。该算法从一组初始基因开始,逐步向交互网络中添加候选基因,并在确定x不能导致有效解时放弃每个候选x。排除向量(EV)用于完成此任务,并在每一步填充,维护未来需要从交互中排除的节点列表,从而限制网络的大小。EV还可以通过使用基因本体(GO)单元组件分类来丢弃与网络无关的节点,从而实现位置感知。该算法可以很容易地应用于途径分析和确定细胞间相互作用的要素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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