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A Minimum-Labeling Approach for Reconstructing Protein Networks across Multiple Conditions

机译:跨多种条件重建蛋白质网络的最小标签方法

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The sheer amounts of biological data that are generated in recent years have driven the development of network analysis tools to facilitate the interpretation and representation of these data. A fundamental challenge in this domain is the reconstruction of a protein-protein subnetwork that underlies a process of interest from a genome-wide screen of associated genes. Despite intense work in this area, current algorithmic approaches are largely limited to analyzing a single screen and are, thus, unable to account for information on condition-specific genes, or reveal the dynamics (over time or condition) of the process in question. Here we propose a novel formulation for network reconstruction from multiple-condition data and devise an efficient integer program solution for it. We apply our algorithm to analyze the response to influenza infection in humans over time as well as to analyze a pair of ER export related screens in humans. By comparing to an extant, single-condition tool we demonstrate the power of our new approach in integrating data from multiple conditions in a compact and coherent manner, capturing the dynamics of the underlying processes.
机译:近年来产生的大量生物学数据推动了网络分析工具的发展,以促进这些数据的解释和表示。这个领域的一个基本挑战是蛋白质-蛋白质子网络的重建,该网络是相关基因全基因组筛选中感兴趣的过程的基础。尽管在该领域进行了大量工作,但是当前的算法方法在很大程度上仅限于分析单个屏幕,因此无法解释有关条件特定基因的信息,也无法揭示所讨论过程的动态性(随时间或条件变化)。在这里,我们提出了一种用于从多条件数据进行网络重构的新颖公式,并为此设计了一种有效的整数程序解决方案。我们应用我们的算法来分析人类对流感感染的反应,以及分析人类与ER出口相关的一对屏幕。通过与现存的单条件工具进行比较,我们展示了我们的新方法的强大功能,它以紧凑和一致的方式集成了来自多个条件的数据,并捕获了基础流程的动态。

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