Evidence map›Paper›PMID 39678204›Full record

ArticleBioinformatics advances2024

Population-aware permutation-based significance thresholds for genome-wide association studies.

Maura John, Arthur Korte, Marco Todesco, Dominik G Grimm

Abstract read
In one paragraph

Article in Bioinformatics advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. The Paraphyletic Origins of Genetic Resistance to Cabbage Stem Flea Beetle inPlant-environment interactions (Hoboken, N.J.) · 2026
    Article
  2. Frontiers in plant science · 2026
    Article
  3. FlexLMM: a Nextflow linear mixed model framework for GWAS.Bioinformatics (Oxford, England) · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Maura JohnTechnical University of Munich, TUM Campus Straubing for Biotechnology and Sustainability, Bioinformatics, 94315 Straubing, Germany.ORCID https://orcid.org/0000-0002-2773-2426
Arthur KorteFaculty of Biology, University of Würzburg, 97074 Würzburg, Germany.ORCID https://orcid.org/0000-0003-0831-1463
Marco TodescoMichael Smith Laboratories, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Dominik G GrimmTechnical University of Munich, TUM Campus Straubing for Biotechnology and Sustainability, Bioinformatics, 94315 Straubing, Germany.ORCID https://orcid.org/0000-0003-2085-4591

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Permutation-based significance thresholds have been shown to be a robust alternative to classical Bonferroni significance thresholds in genome-wide association studies (GWAS) for skewed phenotype distributions. The recently published method permGWAS introduced a batch-wise approach to efficiently compute permutation-based GWAS. However, running multiple univariate tests in parallel leads to many repetitive computations and increased computational resources. More importantly, traditional permutation methods that permute only the phenotype break the underlying population structure. Results: We propose permGWAS2, an improved method that does not break the population structure during permutations and uses an elegant block matrix decomposition to optimize computations, thereby reducing redundancies. We show on synthetic data that this improved approach yields a lower false discovery rate for skewed phenotype distributions compared to the previous version and the commonly used Bonferroni correction. In addition, we re-analyze a dataset covering phenotypic variation in 86 traits in a population of 615 wild sunflowers ( Availability and implementation: permGWAS2 is open-source and publicly available on GitHub for download: https://github.com/grimmlab/permGWAS.

Identifiers

PMID39678204
PMCPMC11639184

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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.