Abstract

BackgroundPermutation testing is often considered the “gold standard” for multi-test significance analysis, as it is an exact test requiring few assumptions about the distribution being computed. However, it can be computationally very expensive, particularly in its naive form in which the full analysis pipeline is re-run after permuting the phenotype labels. This can become intractable in multi-locus genome-wide association studies (GWAS), in which the number of potential interactions to be tested is combinatorially large.ResultsIn this paper, we develop an approach for permutation testing in multi-locus GWAS, specifically focusing on SNP–SNP-phenotype interactions using multivariable measures that can be computed from frequency count tables, such as those based in Information Theory. We find that the computational bottleneck in this process is the construction of the count tables themselves, and that this step can be eliminated at each iteration of the permutation testing by transforming the count tables directly. This leads to a speed-up by a factor of over 103 for a typical permutation test compared to the naive approach. Additionally, this approach is insensitive to the number of samples making it suitable for datasets with large number of samples.ConclusionsThe proliferation of large-scale datasets with genotype data for hundreds of thousands of individuals enables new and more powerful approaches for the detection of multi-locus genotype-phenotype interactions. Our approach significantly improves the computational tractability of permutation testing for these studies. Moreover, our approach is insensitive to the large number of samples in these modern datasets. The code for performing these computations and replicating the figures in this paper is freely available at https://github.com/kunert/permute-counts.

Highlights

  • Permutation testing is often considered the “gold standard” for multitest significance analysis, as it is an exact test requiring few assumptions about the distribution being computed

  • Genome-wide association studies (GWAS) have shed light on the genetics of complex traits and diseases, but single-locus analyses fail to detect the epistatic gene–gene interactions, which play a crucial role in the genetics of complex traits [1,2,3]

  • We focus here on the class of techniques based on information theory, which formulate entropy-based measures sensitive to multi-gene epistatic interactions

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Summary

Introduction

Permutation testing is often considered the “gold standard” for multitest significance analysis, as it is an exact test requiring few assumptions about the distribution being computed It can be computationally very expensive, in its naive form in which the full analysis pipeline is re-run after permut‐ ing the phenotype labels. We focus here on the class of techniques based on information theory, which formulate entropy-based measures sensitive to multi-gene epistatic interactions These approaches are powerful due to being inherently model-free and sensitive to nonlinear relationships [3]. Permutation testing is often considered the “gold standard” for multi-test significance analysis [32, 33], and is the approach utilized by the majority of the above studies [20,21,22,23,24,25,26,27, 29, 34, 35]

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