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Precision-based sample size reduction for Bayesian experimentation using Markov chain simulation.

机译:使用马尔可夫链模拟进行贝叶斯实验的基于精度的样本量减少。

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摘要

The costs of sampling are often quite high in biomedical engineering and medicine, where collecting data is often invasive, destructive, or time consuming. This results in experiments that are either sparse or very expensive. Optimal design strategies can help a researcher to make the most of a given number of experimental observations, but neglect the actual problem of sample size determination. For a grey-box experiment with continuous parameter and observation spaces, one must determine how many observations are required in order to ensure precise parameter estimates that resist experimental error and prior uncertainty in the parameter values. This work proposes a novel approach to sample size determination that bridges experimental science with principles of quality engineering and control. Parallel Markov chains are simulated from the prior and preposterior distributions to generate posterior predictive distributions for a proposed experiment. This represents the population of possible posterior distributions for the experiment over the entire observation space. One can compute the expected estimator precision and determine the optimal sample size as a measure of the "consumer's risk", i.e., the probability that the experiment, on the average, will fail to yield a necessary degree of estimator precision. This work evaluates the proposed method by applying it to a combination of simulated and practical experiments, which validate the utility of the algorithm and examine its properties under various prior distributions and degrees of experimental error. This work also created a specialized software package to carry out the computations necessary for sample size determination.
机译:在生物医学工程和医学中,采样的成本通常很高,在这些地方采集数据通常是侵入性的,破坏性的或耗时的。这导致实验稀疏或非常昂贵。最佳设计策略可以帮助研究人员充分利用给定数量的实验观察结果,而忽略了样本量确定的实际问题。对于具有连续参数和观测空间的灰盒实验,必须确定需要进行多少观测才能确保精确的参数估算值能够抵抗实验误差和参数值先前的不确定性。这项工作提出了一种确定样本量的新方法,该方法将实验科学与质量工程和控制原理联系起来。从先验和后验分布模拟并行马尔可夫链,以为拟议的实验生成后验预测分布。这代表了整个观察空间中实验可能的后验分布的总体。可以计算出预期的估算器精度,并确定最佳的样本量作为“消费者风险”的一种度量,即平均而言该实验将无法产生必要程度的估算器精度的概率。这项工作通过将其应用于模拟和实际实验相结合的方法来评估所提出的方法,该方法验证了该算法的实用性并在各种先验分布和实验误差程度下检查了其性能。这项工作还创建了一个专门的软件包,以执行确定样本量所需的计算。

著录项

  • 作者

    Huber, David J.;

  • 作者单位

    University of Southern California.;

  • 授予单位 University of Southern California.;
  • 学科 Engineering Biomedical.;Statistics.;Mathematics.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 318 p.
  • 总页数 318
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:39:27

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