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首页> 外文期刊>BMC Bioinformatics >Bottom-up GGM algorithm for constructing multilayered hierarchical gene regulatory networks that govern biological pathways or processes
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Bottom-up GGM algorithm for constructing multilayered hierarchical gene regulatory networks that govern biological pathways or processes

机译:自下而上的GGM算法,用于构建控制生物学途径或过程的多层层次基因调控网络

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Background Multilayered hierarchical gene regulatory networks (ML-hGRNs) are very important for understanding genetics regulation of biological pathways. However, there are currently no computational algorithms available for directly building ML-hGRNs that regulate biological pathways. Results A bottom-up graphic Gaussian model (GGM) algorithm was developed for constructing ML-hGRN operating above a biological pathway using small- to medium-sized microarray or RNA-seq data sets. The algorithm first placed genes of a pathway at the bottom layer and began to construct a ML-hGRN by evaluating all combined triple genes: two pathway genes and one regulatory gene. The algorithm retained all triple genes where a regulatory gene significantly interfered two paired pathway genes. The regulatory genes with highest interference frequency were kept as the second layer and the number kept is based on an optimization function. Thereafter, the algorithm was used recursively to build a ML-hGRN in layer-by-layer fashion until the defined number of layers was obtained or terminated automatically. Conclusions We validated the algorithm and demonstrated its high efficiency in constructing ML-hGRNs governing biological pathways. The algorithm is instrumental for biologists to learn the hierarchical regulators associated with a given biological pathway from even small-sized microarray or RNA-seq data sets.
机译:背景技术多层层次基因调控网络(ML-hGRNs)对于理解生物学途径的遗传调控非常重要。但是,目前尚无可用于直接构建调节生物学途径的ML-hGRN的计算算法。结果开发了一种自下而上的图形高斯模型(GGM)算法,用于使用中小型阵列或RNA-seq数据集构建在生物学途径之上运行的ML-hGRN。该算法首先将路径的基因置于底层,然后通过评估所有组合的三重基因:两个路径基因和一个调节基因,开始构建ML-hGRN。该算法保留了所有三重基因,其中调节基因显着干扰了两个成对的途径基因。将具有最高干扰频率的调控基因保留为第二层,保留的数目基于优化函数。之后,递归使用该算法以逐层方式构建ML-hGRN,直到自动获得或终止定义的层数为止。结论我们验证了该算法并证明了其在构建调控生物途径的ML-hGRNs中的高效性。该算法对于生物学家从小规模的微阵列或RNA-seq数据集中学习与给定生物途径相关的分级调节器非常有用。

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