A simple and flexible test of sample exchangeability with applications to statistical genomics

TL;DR

The paper introduces the V test, a simple, fast, and flexible non-parametric method for testing sample exchangeability and feature independence in multivariate data, with applications in statistical genomics.

Contribution

It proposes a novel non-parametric V test that addresses sample exchangeability and feature independence, controlling Type I error and handling high-dimensional data effectively.

Findings

The V test performs well across various simulation scenarios.

It compares favorably against existing stratification tests based on random matrix theory.

Application to genomic data demonstrates practical utility in assessing exchangeability and LD splits.

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 p-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).