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ROBUST IDENTIFICATION OF LARGE GENETIC NETWORKS

机译:大型遗传网络的鲁棒识别

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Temporal and spatial gene expression, together with the concentration of proteins and metabolites, is tightly controlled in the cell. This is possible thanks to complex regulatory networks between these different elements. The identification of these networks would be extremely valuable. We developed a novel algorithm to identify a large genetic network, as a set of linear differential equations, starting from measurements of gene expression at steady state following transcriptional perturbations. Experimentally, it is possible to overexpress each of the genes in the network using an episomal expression plasmid and measure the change in mRNA concentration of all the genes, following the perturbation. Computationally, we reduced the identification problem to a multiple linear regression, assuming that the network is sparse. We implemented a heuristic search method in order to apply the algorithm to large networks. The algorithm can correctly identify the network, even in the presence of large noise in the data, and can be used to predict the genes that directly mediate the action of a compound. Our novel approach is experimentally feasible and it is readily applicable to large genetic networks.
机译:时间和空间基因表达与蛋白质和代谢物的浓度一起在细胞中紧密控制。由于这些不同元素之间的复杂监管网络,这是可能的。这些网络的识别是非常有价值的。我们开发了一种识别大型遗传网络的新算法,作为一组线性微分方程,从转录扰动后稳态的基因表达的测量开始。通过实验,可以使用异构体表达质粒过度抑制网络中的每一个基因,并在扰动后测量所有基因的mRNA浓度的变化。计算地,假设网络稀疏,我们将识别问题减少到多个线性回归。我们实现了一种启发式搜索方法,以便将算法应用于大型网络。算法可以正确地识别网络,即使存在大的数据噪声,也可用于预测直接介导化合物作用的基因。我们的新方法是通过实验可行的,并且随时适用于大型遗传网络。

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