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Bayesian Methods for Variable Selection in Survival Models with Application to DNA Microarray Data

机译:生存模型中的变量选择的贝叶斯方法及其在DNA芯片数据中的应用

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Selection of significant genes via expression patterns is important in a mi-croarray problem. Owing to small sample size and large number of variables (genes), the selection process can be unstable. This paper considers hierarchical Bayesian gene selection model for survival data. In survival analysis the popular models are usually well suited for data with few covariates and many observations (subjects). In contrast for a typical setting of gene expression data from DNA microarray, we need to consider the case where the number of covariates p exceeds the number of samples n. For a given vector of response values which are times to event (death or censored times) and p gene expressions (covariates), we address the issue of how to reduce the dimension by selecting the significant genes. This approach enables us to estimate the survival curve when n < < p. In our approach, rather than fixing the number of selected genes, we assign a prior distribution to this number. That way it creates additional flexibility by allowing the imposition of constraints, such as bounding the dimension via a prior, which in effect works as a penalty. To implement our methodology, we use a Markov Chain Monte Carlo (MCMC) method. We demonstrate the use of the methodology to diffuse large B-cell lymphoma (DLBCL) complementary DNA (cDNA) data and Breast Carcinomas data.
机译:通过表达模式选择重要基因在微阵列问题中很重要。由于样本量小和大量变量(基因),选择过程可能不稳定。本文考虑了用于生存数据的分级贝叶斯基因选择模型。在生存分析中,流行的模型通常非常适合于协变量少,观察值(对象)多的数据。相反,对于来自DNA微阵列的基因表达数据的典型设置,我们需要考虑以下情况:协变量p的数量超过样本n的数量。对于给定的响应值载体,该响应值是事件发生时间(死亡或审查时间)和p基因表达(协变量)的大小,我们解决了如何通过选择重要基因来减少维度的问题。当n p时,这种方法使我们能够估计生存曲线。在我们的方法中,我们不固定选定基因的数目,而是给该数目分配先验分布。这样,它通过允许施加约束(例如通过先验限制尺寸)来创建额外的灵活性,这实际上是一种惩罚。为了实现我们的方法,我们使用马尔可夫链蒙特卡洛(MCMC)方法。我们证明了该方法的使用,以弥散大B细胞淋巴瘤(DLBCL)互补DNA(cDNA)数据和乳腺癌数据。

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