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Hub-Centered Gene Network Reconstruction Using Automatic Relevance Determination

机译:基于自动相关性确定的以枢纽为中心的基因网络重建

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摘要

Network inference deals with the reconstruction of biological networks from experimental data. A variety of different reverse engineering techniques are available; they differ in the underlying assumptions and mathematical models used. One common problem for all approaches stems from the complexity of the task, due to the combinatorial explosion of different network topologies for increasing network size. To handle this problem, constraints are frequently used, for example on the node degree, number of edges, or constraints on regulation functions between network components. We propose to exploit topological considerations in the inference of gene regulatory networks. Such systems are often controlled by a small number of hub genes, while most other genes have only limited influence on the network's dynamic. We model gene regulation using a Bayesian network with discrete, Boolean nodes. A hierarchical prior is employed to identify hub genes. The first layer of the prior is used to regularize weights on edges emanating from one specific node. A second prior on hyperparameters controls the magnitude of the former regularization for different nodes. The net effect is that central nodes tend to form in reconstructed networks. Network reconstruction is then performed by maximization of or sampling from the posterior distribution. We evaluate our approach on simulated and real experimental data, indicating that we can reconstruct main regulatory interactions from the data. We furthermore compare our approach to other state-of-the art methods, showing superior performance in identifying hubs. Using a large publicly available dataset of over 800 cell cycle regulated genes, we are able to identify several main hub genes. Our method may thus provide a valuable tool to identify interesting candidate genes for further study. Furthermore, the approach presented may stimulate further developments in regularization methods for network reconstruction from data.
机译:网络推论涉及根据实验数据重建生物网络。可以使用多种不同的逆向工程技术。它们在所使用的基本假设和数学模型方面有所不同。对于所有方法来说,一个普遍的问题是任务的复杂性,这归因于不同网络拓扑结构的组合爆炸,以增加网络规模。为了解决这个问题,经常使用约束,例如节点度,边数或网络组件之间的调节功能约束。我们建议在推断基因调控网络时利用拓扑考虑。这样的系统通常由少数的集线器基因控制,而大多数其他基因对网络动态的影响有限。我们使用具有离散布尔节点的贝叶斯网络对基因调控进行建模。采用分级先验来鉴定中心基因。先验的第一层用于调整从一个特定节点发出的边缘上的权重。超参数的第二个先验值控制不同节点的前一个正则化幅度。最终结果是中心节点倾向于在重构网络中形成。然后通过最大化后验分布或从后验分布采样来执行网络重构。我们在模拟和真实实验数据上评估我们的方法,表明我们可以从数据中重建主要的监管相互作用。此外,我们将我们的方法与其他最新方法进行了比较,显示出在识别集线器方面的卓越性能。使用超过800个细胞周期调控基因的大型公共数据集,我们能够确定几个主要的中枢基因。因此,我们的方法可能提供了一种有价值的工具,可用于识别有趣的候选基因以供进一步研究。此外,提出的方法可能会刺激用于根据数据进行网络重建的正则化方法的进一步发展。

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