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Estimating Genome-Wide Gene Networks Using Nonparametric Bayesian Network Models on Massively Parallel Computers

机译:在大规模并行计算机上使用非参数贝叶斯网络模型估算全基因组基因网络

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We present a novel algorithm to estimate genome-wide gene networks consisting of more than 20,000 genes from gene expression data using nonparametric Bayesian networks. Due to the difficulty of learning Bayesian network structures, existing algorithms cannot be applied to more than a few thousand genes. Our algorithm overcomes this limitation by repeatedly estimating subnetworks in parallel for genes selected by neighbor node sampling. Through numerical simulation, we confirmed that our algorithm outperformed a heuristic algorithm in a shorter time. We applied our algorithm to microarray data from human umbilical vein endothelial cells (HUVECs) treated with siRNAs, to construct a human genome-wide gene network, which we compared to a small gene network estimated for the genes extracted using a traditional bioinformatics method. The results showed that our genome-wide gene network contains many features of the small network, as well as others that could not be captured during the small network estimation. The results also revealed master-regulator genes that are not in the small network but that control many of the genes in the small network. These analyses were impossible to realize without our proposed algorithm.
机译:我们提出了一种新颖的算法,可以估计使用非参数贝叶斯网络从基因表达数据中的超过20,000个基因组成的全基因组基因网络。由于学习贝叶斯网络结构的困难,现有算法无法应用于数千个基因。我们的算法通过为相邻节点采样选择的基因并行地并行估计子网来克服此限制。通过数值模拟,我们证实了我们的算法在较短的时间内优于启发式算法。我们将我们的算法应用到经过siRNA处理的人脐静脉内皮细胞(HUVEC)的微阵列数据中,构建了一个全基因组的基因网络,我们将其与使用传统生物信息学方法提取的基因估计的小型基因网络进行了比较。结果表明,我们的全基因组基因网络包含小型网络的许多功能,以及在小型网络估算期间无法捕获的其他功能。结果还揭示了不在小型网络中但控制小型网络中许多基因的主调控基因。如果没有我们提出的算法,这些分析是不可能实现的。

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