{"title":"A SIMPLE AND FLEXIBLE TEST OF SAMPLE EXCHANGEABILITY WITH APPLICATIONS TO STATISTICAL GENOMICS.","authors":"Alan J Aw, Jeffrey P Spence, Yun S Song","doi":"10.1214/23-aoas1817","DOIUrl":null,"url":null,"abstract":"<p><p>In scientific studies involving analyses of multivariate data, basic but important questions often arise for the researcher: Is the sample exchangeable, meaning that the joint distribution of the sample is invariant to the ordering of the units? Are the features independent of one another, or perhaps the features can be grouped so that the groups are mutually independent? In statistical genomics, these considerations are fundamental to downstream tasks such as demographic inference and the construction of polygenic risk scores. We propose a non-parametric approach, which we call the V test, to address these two questions, namely, a test of sample exchangeability given dependency structure of features, and a test of feature independence given sample exchangeability. Our test is conceptually simple, yet fast and flexible. It controls the Type I error across realistic scenarios, and handles data of arbitrary dimensions by leveraging large-sample asymptotics. Through extensive simulations and a comparison against unsupervised tests of stratification based on random matrix theory, we find that our test compares favorably in various scenarios of interest. We apply the test to data from the 1000 Genomes Project, demonstrating how it can be employed to assess exchangeability of the genetic sample, or find optimal linkage disequilibrium (LD) splits for downstream analysis. For exchangeability assessment, we find that removing rare variants can substantially increase the <math><mi>p</mi></math>-value of the test statistic. For optimal LD splitting, the V test reports different optimal splits than previous approaches not relying on hypothesis testing. Software for our methods is available in R (CRAN: flintyR) and Python (PyPI: flintyPy).</p>","PeriodicalId":50772,"journal":{"name":"Annals of Applied Statistics","volume":"18 1","pages":"858-881"},"PeriodicalIF":1.3000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11115382/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Applied Statistics","FirstCategoryId":"100","ListUrlMain":"https://doi.org/10.1214/23-aoas1817","RegionNum":4,"RegionCategory":"数学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/31 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"STATISTICS & PROBABILITY","Score":null,"Total":0}
引用次数: 0
Abstract
In scientific studies involving analyses of multivariate data, basic but important questions often arise for the researcher: Is the sample exchangeable, meaning that the joint distribution of the sample is invariant to the ordering of the units? Are the features independent of one another, or perhaps the features can be grouped so that the groups are mutually independent? In statistical genomics, these considerations are fundamental to downstream tasks such as demographic inference and the construction of polygenic risk scores. We propose a non-parametric approach, which we call the V test, to address these two questions, namely, a test of sample exchangeability given dependency structure of features, and a test of feature independence given sample exchangeability. Our test is conceptually simple, yet fast and flexible. It controls the Type I error across realistic scenarios, and handles data of arbitrary dimensions by leveraging large-sample asymptotics. Through extensive simulations and a comparison against unsupervised tests of stratification based on random matrix theory, we find that our test compares favorably in various scenarios of interest. We apply the test to data from the 1000 Genomes Project, demonstrating how it can be employed to assess exchangeability of the genetic sample, or find optimal linkage disequilibrium (LD) splits for downstream analysis. For exchangeability assessment, we find that removing rare variants can substantially increase the -value of the test statistic. For optimal LD splitting, the V test reports different optimal splits than previous approaches not relying on hypothesis testing. Software for our methods is available in R (CRAN: flintyR) and Python (PyPI: flintyPy).
在涉及多变量数据分析的科学研究中,研究人员经常会遇到一些基本但重要的问题: 样本是否可交换,即样本的联合分布与单位排序无关?特征是否相互独立,或者特征是否可以分组,从而使各组相互独立?在统计基因组学中,这些考虑因素对于人口推断和构建多基因风险评分等下游任务至关重要。我们提出了一种非参数方法(我们称之为 V 检验)来解决这两个问题,即给定特征依赖结构的样本可交换性检验和给定样本可交换性的特征独立性检验。我们的检验方法概念简单、快速灵活。它能在现实场景中控制 I 类误差,并利用大样本渐近学处理任意维度的数据。通过大量的模拟以及与基于随机矩阵理论的无监督分层检验的比较,我们发现我们的检验在各种感兴趣的情况下都表现出色。我们将该检验应用于 1000 基因组计划的数据,展示了如何利用它来评估基因样本的可交换性,或为下游分析找到最佳的连锁不平衡(LD)分割。在可交换性评估中,我们发现去除罕见变异可大幅提高检验统计量的 p 值。对于最优 LD 分割,V 检验报告的最优分割与之前不依赖假设检验的方法不同。我们的方法可在 R(CRAN:flintyR)和 Python(PyPI:flintyPy)中使用。
期刊介绍:
Statistical research spans an enormous range from direct subject-matter collaborations to pure mathematical theory. The Annals of Applied Statistics, the newest journal from the IMS, is aimed at papers in the applied half of this range. Published quarterly in both print and electronic form, our goal is to provide a timely and unified forum for all areas of applied statistics.