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AI 根据所提供的论文材料归类:摘要研究空间区域的选择后推断;未涉及网络干扰、因果识别或其他给定细分。

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关注这篇论文的作者
Yuval Benjamini
Jonathan Taylor
Rafael A. Irizarry

高通量检测中区域识别的选择校正统计推断

研究问题
将超过阈值的相邻位置合并为信号区域后,如何校正区域选择偏差,为区域总体平均效应提供可信的估计与区间?
方法与思路
作者提出pin-down推断,在匹配选择约束的截断条件单参数指数族中进行区域推断,并通过二次筛选与调整控制错误覆盖率。
材料陈述的贡献
摘要称方法提供校正局部选择偏差的非渐近点估计与区间,容纳非平稳协方差,并对报告区域集合控制错误覆盖率。
阅读关注点
应核对区域选择事件及条件化对象、协方差如何获得,以及区域平均效应定义和二次筛选后的错误覆盖率保证。
阅读边界
仅据版本未注明的OpenAlex摘要;分布模型、协方差处理和有限样本保证条件未详述,区域效应不自动具有因果解释。

原文摘要

Scientists use high-dimensional measurement assays to detect and prioritize regions of strong signal in spatially organized domain. Examples include finding methylation enriched genomic regions using microarrays, and active cortical areas using brain-imaging. The most common procedure for detecting potential regions is to group neighboring sites where the signal passed a threshold. However, one needs to account for the selection bias induced by this procedure to avoid diminishing effects when generalizing to a population. This paper introduces pin-down inference, a model and an inference framework that permit population inference for these detected regions. Pin-down inference provides non-asymptotic point and confidence interval estimators for the mean effect in the region that account for local selection bias. Our estimators accommodate non-stationary covariances that are typical of these data, allowing researchers to better compare regions of different sizes and correlation structures. Inference is provided within a conditional one-parameter exponential family per region, with truncations that match the selection constraints. A secondary screening-and-adjustment step allows pruning the set of detected regions, while controlling the false-coverage rate over the reported regions. We apply the method to genomic regions with differing DNA-methylation rates across tissue. Our method provides superior power compared to other conditional and non-parametric approaches.

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