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Inferring metabolic networks using the Bayesian adaptive graphical lasso with informative priors

机译:使用贝叶斯自适应图形套索和信息先验推断代谢网络

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摘要

Metabolic processes are essential for cellular function and survival. We are interested in inferring a metabolic network in activated microglia, a major neuroimmune cell in the brain responsible for the neuroinflammation associated with neurological diseases, based on a set of quantified metabolites. To achieve this, we apply the Bayesian adaptive graphical lasso with informative priors that incorporate known relationships between covariates. To encourage sparsity, the Bayesian graphical lasso places double exponential priors on the off-diagonal entries of the precision matrix. The Bayesian adaptive graphical lasso allows each double exponential prior to have a unique shrinkage parameter. These shrinkage parameters share a common gamma hyperprior. We extend this model to create an informative prior structure by formulating tailored hyperpriors on the shrinkage parameters. By choosing parameter values for each hyperprior that shift probability mass toward zero for nodes that are close together in a reference network, we encourage edges between covariates with known relationships. This approach can improve the reliability of network inference when the sample size is small relative to the number of parameters to be estimated. When applied to the data on activated microglia, the inferred network includes both known relationships and associations of potential interest for further investigation.
机译:代谢过程对于细胞功能和生存至关重要。我们对基于一组定量代谢物推断活化小胶质细胞的代谢网络感兴趣,小胶质细胞是大脑中负责与神经系统疾病相关的神经炎症的主要神经免疫细胞。为了实现这一目标,我们将贝叶斯自适应图形套索与信息先验相结合,并结合了协变量之间的已知关系。为鼓励稀疏性,贝叶斯图形套索将双指数先验值放在精度矩阵的非对角项上。贝叶斯自适应图形套索允许每个双指数具有唯一的收缩参数。这些收缩参数具有共同的伽玛优先级。我们通过在收缩参数上制定量身定做的超优先级,扩展该模型以创建信息丰富的先验结构。通过为每个超优先级选择参数值,以使参考网络中彼此靠近的节点的概率质量朝零移动,我们鼓励具有已知关系的协变量之间的边。当样本大小相对于要估计的参数数量较小时,此方法可以提高网络推断的可靠性。当应用于激活的小胶质细胞上的数据时,推断的网络将同时包含已知的关系和潜在兴趣的关联,以供进一步研究。

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