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Stability of Inferring Gene Regulatory Structure with Dynamic Bayesian Networks

机译:动态贝叶斯网络推断基因监管结构的稳定性

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Though a plethora of techniques have been used to build gene regulatory networks (GRN) from time-series gene expression data, stabilities of such techniques have not been studied. This paper investigates the stability of GRN built using dynamic Bayesian networks (DBN) by synthetically generating gene expression time-series. Assuming scale-free topologies, sample datasets are drawn from DBN to evaluate the stability of estimating the structure of GRN. Our experiments indicate although high accuracy can be achieved with equal number of time points to the number of genes in the network, the presence of large numbers of false positives and false negatives deteriorate the stability of building GRN. The stability could be improved by gathering gene expression at more time points. Interestingly, large networks required less number of time points (normalized to the size of the network) than small networks to achieve the same level stability.
机译:虽然已经用于从时间序列基因表达数据中用于构建基因调节网络(GRN)的血清技术,但尚未研究这些技术的稳定性。本文通过综合生成基因表达时间序列,研究了使用动态贝叶斯网络(DBN)建造的GRN的稳定性。假设无尺度拓扑,从DBN中汲取样本数据集以评估估计GRN结构的稳定性。我们的实验表明,尽管通过相同数量的时间指向网络中基因数量的高精度可以实现高精度,但大量的假阳性和假阴性的存在会使建筑物的稳定性恶化。通过在更多时间点收集基因表达可以改善稳定性。有趣的是,大型网络需要少量的时间点(标准化为网络大小),而不是小型网络实现相同的级别稳定性。

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