Fast Exact Bayesian Inference for Sparse Signals in the Normal Sequence Model.

T. Erven, Botond Szabó
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引用次数: 7

Abstract

We consider exact algorithms for Bayesian inference with model selection priors (including spike-and-slab priors) in the sparse normal sequence model. Because the best existing exact algorithm becomes numerically unstable for sample sizes over n=500, there has been much attention for alternative approaches like approximate algorithms (Gibbs sampling, variational Bayes, etc.), shrinkage priors (e.g. the Horseshoe prior and the Spike-and-Slab LASSO) or empirical Bayesian methods. However, by introducing algorithmic ideas from online sequential prediction, we show that exact calculations are feasible for much larger sample sizes: for general model selection priors we reach n=25000, and for certain spike-and-slab priors we can easily reach n=100000. We further prove a de Finetti-like result for finite sample sizes that characterizes exactly which model selection priors can be expressed as spike-and-slab priors. Finally, the computational speed and numerical accuracy of the proposed methods are demonstrated in experiments on simulated data and on a prostate cancer data set. In our experimental evaluation we compute guaranteed bounds on the numerical accuracy of all new algorithms, which shows that the proposed methods are numerically reliable whereas an alternative based on long division is not.
正态序列模型中稀疏信号的快速精确贝叶斯推断。
我们考虑了稀疏正态序列模型中具有模型选择先验(包括尖峰-板先验)的贝叶斯推理的精确算法。由于现有的最佳精确算法对于超过n=500的样本量在数值上变得不稳定,因此有很多人关注替代方法,如近似算法(吉布斯抽样,变分贝叶斯等),收缩先验(例如马蹄先验和钉板LASSO)或经验贝叶斯方法。然而,通过引入在线序列预测的算法思想,我们表明精确的计算对于更大的样本量是可行的:对于一般的模型选择先验,我们达到n=25000,对于某些spike-and-slab先验,我们可以轻松达到n=100000。对于有限样本量,我们进一步证明了一个类似于de finetti的结果,该结果准确地表征了哪些模型选择先验可以表示为尖峰-板先验。最后,在模拟数据和前列腺癌数据集上进行了实验,验证了所提方法的计算速度和数值精度。在我们的实验评估中,我们计算了所有新算法数值精度的保证边界,这表明所提出的方法在数值上是可靠的,而基于长除法的替代方法则不是。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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