k-PathA: k-shortest Path Algorithm

Alexander Ullrich, C. Forst
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引用次数: 6

Abstract

One important aspect of computational systems biology includes the identification and analysis of functional response networks within large biochemical networks. These functional response networks represent the response of a biological system under a particular experimental condition which can be used to pinpoint critical biological processes.For this purpose, we have developed a novel algorithm to calculate response networks as scored/weighted sub-graphs spanned by k-shortest simple (loop free) paths. The k-shortest simple path algorithm is based on a forward/backward chaining approach synchronized between pairs of processors. The algorithm scales linear with the number of processors used. The algorithm implementation is using a Linux cluster platform, MPI lam and mpiJava messaging as well as the Java language for the application.The algorithm is performed on a hybrid human network consisting of 45,041 nodes and 438,567 interactions together with gene expression information obtained from human cell-lines infected by influenza virus. Its response networks show the early innate immune response and virus triggered processes within human epithelial cells. Especially under the imminent threat of a pandemic caused by novel influenza strains, such as the current H1N1 strain, these analyses are crucial for a comprehensive understanding of molecular processes during early phases of infection. Such a systems level understanding may aid in the identification of therapeutic markers and in drug development for diagnosis and finally prevention of a potentially dangerous disease.
k-PathA: k最短路径算法
计算系统生物学的一个重要方面包括识别和分析大型生化网络中的功能响应网络。这些功能反应网络代表了生物系统在特定实验条件下的反应,可用于查明关键的生物过程。为此,我们开发了一种新的算法,将响应网络计算为由k最短简单(无循环)路径跨越的评分/加权子图。k-最短简单路径算法基于处理器对之间同步的正向/反向链方法。该算法与所使用的处理器数量成线性关系。算法的实现采用Linux集群平台,MPI lam和mpiJava消息传递以及Java语言进行应用。该算法在由45,041个节点和438,567个相互作用组成的混合人类网络上执行,并从感染流感病毒的人类细胞系中获得基因表达信息。它的应答网络显示了早期的先天免疫应答和病毒在人上皮细胞内触发的过程。特别是在新型流感毒株(如当前的H1N1毒株)引起的大流行迫在眉睫的威胁下,这些分析对于全面了解感染早期阶段的分子过程至关重要。这种系统级的理解可能有助于识别治疗标记物和用于诊断和最终预防潜在危险疾病的药物开发。
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