Evidence map›Paper›PMID 31198442›Full record

ArticleBioData mining2019

Confounding of linkage disequilibrium patterns in large scale DNA based gene-gene interaction studies.

Marc Joiret, Jestinah M Mahachie John, Elena S Gusareva, Kristel Van Steen

Erratum issuedAbstract read
In one paragraph

Article in BioData mining, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

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  7. Genome-wide association study ofFrontiers in plant science · 2024
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  12. Genes · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Marc JoiretBIO3, GIGA-R Medical Genomics, Avenue de l'Hôpital 1-B34-CHU, Liège, 4000 Belgium.ORCID 0000-0001-5381-4196
Jestinah M Mahachie JohnBIO3, GIGA-R Medical Genomics, Avenue de l'Hôpital 1-B34-CHU, Liège, 4000 Belgium.
Elena S GusarevaBIO3, GIGA-R Medical Genomics, Avenue de l'Hôpital 1-B34-CHU, Liège, 4000 Belgium.
Kristel Van SteenBIO3, GIGA-R Medical Genomics, Avenue de l'Hôpital 1-B34-CHU, Liège, 4000 Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Genome-Wide Association Studies (GWAS), the concept of linkage disequilibrium is important as it allows identifying genetic markers that tag the actual causal variants. In Genome-Wide Association Interaction Studies (GWAIS), similar principles hold for pairs of causal variants. However, Linkage Disequilibrium (LD) may also interfere with the detection of genuine epistasis signals in that there may be complete confounding between Gametic Phase Disequilibrium (GPD) and interaction. GPD may involve unlinked genetic markers, even residing on different chromosomes. Often GPD is eliminated in GWAIS, via feature selection schemes or so-called pruning algorithms, to obtain unconfounded epistasis results. However, little is known about the optimal degree of GPD/LD-pruning that gives a balance between false positive control and sufficient power of epistasis detection statistics. Here, we focus on Model-Based Multifactor Dimensionality Reduction as one large-scale epistasis detection tool. Its performance has been thoroughly investigated in terms of false positive control and power, under a variety of scenarios involving different trait types and study designs, as well as error-free and noisy data, but never with respect to multicollinear SNPs.

resultsUsing real-life human LD patterns from a homogeneous subpopulation of British ancestry, we investigated the impact of LD-pruning on the statistical sensitivity of MB-MDR. We considered three different non-fully penetrant epistasis models with varying effect sizes. There is a clear advantage in pre-analysis pruning using sliding windows at

conclusionsOur results confirm that LD patterns and the position of causal variants in LD blocks do have an impact on epistasis detection, and that pruning strategies and LD-blocks definitions combined need careful attention, if we wish to maximize the power of large-scale epistasis screenings.

Indexed as

1000 genomes projectAnkylosing spondylitisGametic phase disequilibrium (GPD)Genome-wide association interaction studies (GWAIS)Model-based multifactor-dimensionality reduction (MB-MDR)Signal sensitivity

Identifiers

PMID31198442
PMCPMC6558841

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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.