Evidence map›Paper›PMID 33827420›Full record

ArticleBMC bioinformatics2021

Optimized permutation testing for information theoretic measures of multi-gene interactions.

James M Kunert-Graf, Nikita A Sakhanenko, David J Galas

Abstract read
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Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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  4. Dissecting the contribution of single nucleotide polymorphisms inJournal of translational autoimmunity · 2021
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

James M Kunert-GrafPacific Northwest Research Institute, 720 Broadway, Seattle, WA, 98122, USA. jkunert@pnri.org.ORCID http://orcid.org/0000-0002-3004-7593
Nikita A SakhanenkoPacific Northwest Research Institute, 720 Broadway, Seattle, WA, 98122, USA.
David J GalasPacific Northwest Research Institute, 720 Broadway, Seattle, WA, 98122, USA.

Funding

Reference Profiles of Extracellular RNA in 4 Body Fluids of Healthy HumansU01HL126496 · NHLBI · PACIFIC NORTHWEST RESEARCH INSTITUTE · PI GALAS, DAVID J., NICKERSON, DEBORAH A · 2014 to 2018
$3.5M
NHLBI NIH HHS U01HL126496
6 · The paper itself

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 10

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 .

Indexed as

Epistasis, GeneticGenome-Wide Association StudyPolymorphism, Single NucleotideGenotypeHumansPhenotypeInformation theoryMulti-locus GWASMultivariable interactionsPermutation testing

Identifiers

PMID33827420
PMCPMC8028212

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.