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Quantifying The Fraction Of Missing Information For Hypothesis Testing In Statistical And Genetic Studies

机译:定量统计和遗传研究中用于假设检验的缺失信息的分数

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Many practical studies rely on hypothesis testing procedures applied to data sets with missing information. An important part of the analysis is to determine the impact of the missing data on the performance of the test, and this can be done by properly quantifying the relative (to complete data) amount of available information. The problem is directly motivated by applications to studies, such as linkage analyses and haplotype-based association projects, designed to identify genetic contributions to complex diseases. In the genetic studies the relative information measures are needed for the experimental design, technology comparison, interpretation of the data, and for understanding the behavior of some of the inference tools. The central difficulties in constructing such information measures arise from the multiple, and sometimes conflicting, aims in practice. For large samples, we show that a satisfactory, likelihood-based general solution exists by using appropriate forms of the relative Kullback-Leibler information, and that the proposed measures are computationally inexpensive given the maximized likelihoods with the observed data. Two measures are introduced, under the null and alternative hypothesis respectively. We exemplify the measures on data coming from mapping studies on the inflammatory bowel disease and diabetes. For small-sample problems, which appear rather frequently in practice and sometimes in disguised forms (e.g., measuring individual contributions to a large study), the robust Bayesian approach holds great promise, though the choice of a general-purpose "default prior" is a very challenging problem. We also report several intriguing connections encountered in our investigation, such as the connection with the fundamental identity for the EM algorithm, the connection with the second CR (Chapman-Robbins) lower information bound, the connection with entropy, and connections between likelihood ratios and Bayes factors. We hope that these seemingly unrelated connections, as well as our specific proposals, will stimulate a general discussion and research in this theoretically fascinating and practically needed area.
机译:许多实践研究依赖于假设检验程序,该程序适用于信息缺失的数据集。分析的重要部分是确定丢失的数据对测试性能的影响,这可以通过适当地量化可用信息的相对量(以完成数据)来完成。该问题是由研究的应用直接引起的,例如连锁分析和基于单倍型的关联项目,这些项目旨在确定对复杂疾病的遗传贡献。在遗传研究中,需要相对信息措施来进行实验设计,技术比较,数据解释以及理解某些推理工具的行为。在实践中,构建这样的信息度量的主要困难来自多个目标,有时是相互矛盾的。对于大样本,我们表明通过使用相对形式的Kullback-Leibler信息的合适形式,存在一种令人满意的,基于似然性的通用解决方案,并且鉴于观察到的数据具有最大的似然性,因此所提出的措施在计算上并不昂贵。在原假设和替代假设下分别引入了两种度量。我们以炎症性肠病和糖尿病的作图研究为例,对数据进行了举例说明。对于小样本问题,在实践中经常出现且有时以变相的形式出现(例如,衡量对大型研究的个人贡献),稳健的贝叶斯方法具有广阔的前景,尽管选择了通用的“默认优先级”一个非常具有挑战性的问题。我们还报告了我们研究中遇到的一些有趣的联系,例如与EM算法的基本身份的联系,与第二CR(Chapman-Robbins)下信息界的联系,与熵的联系以及似然比和贝叶斯因素。我们希望这些看似无关的联系,以及我们的具体建议,将激发这一在理论上令人着迷且实际需要的领域中的一般性讨论和研究。

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