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AI 根据所提供的论文材料归类:摘要核心是蛋白质组多元均值检验,治疗数据应用未提供因果识别框架,也未明确涉及所列其他经济计量方向。

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代码、数据与补充材料

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关注这篇论文的作者
Lin S. Chen
Debashis Paul
Ross L. Prentice
Pei Wang

用于蛋白质组通路分析的正则化 Hotelling T² 检验

研究问题
在样本很小、缺失较多且蛋白质间相关复杂的情况下,如何检验生物通路的多维均值变化,同时控制第一类错误?
方法与思路
作者提出正则化 Hotelling T² 统计量及非参数检验程序,研究其渐近性质,通过模拟比较四种方法,并分析激素治疗数据。
材料陈述的贡献
摘要称,该检验在复杂相关和缺失模式下能控制第一类错误并保持良好功效,实际应用识别出若干血清浓度变化的通路。
阅读关注点
应核对正则化参数、缺失数据处理及非参数校准方式,检查渐近条件与小样本表现,并确认通路多重检验如何处理。
阅读边界
仅据版本未注明的 OpenAlex 索引摘要。缺失机制、正则条件和具体结果未说明,不能将治疗后变化直接解释为因果效应或推断刊本变化。

原文摘要

Recent proteomic studies have identified proteins related to specific phenotypes. In addition to marginal association analysis for individual proteins, analyzing pathways (functionally related sets of proteins) may yield additional valuable insights. Identifying pathways that differ between phenotypes can be conceptualized as a multivariate hypothesis testing problem: whether the mean vector μ of a p-dimensional random vector X is μ0. Proteins within the same biological pathway may correlate with one another in a complicated way, and Type I error rates can be inflated if such correlations are incorrectly assumed to be absent. The inflation tends to be more pronounced when the sample size is very small or there is a large amount of missingness in the data, as is frequently the case in proteomic discovery studies. To tackle these challenges, we propose a regularized Hotelling’s T2 (RHT) statistic together with a nonparametric testing procedure, which effectively controls the Type I error rate and maintains good power in the presence of complex correlation structures and missing data patterns. We investigate asymptotic properties of the RHT statistic under pertinent assumptions and compare the test performance with four existing methods through simulation examples. We apply the RHT test to a hormone therapy proteomics dataset, and identify several interesting biological pathways for which blood serum concentrations changed following hormone therapy initiation. This article has supplementary material online.

笔记与分组
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