Evidence map›Paper›PMID 39792937›Full record

ArticlePLoS genetics2025

ADELLE: A global testing method for trans-eQTL mapping.

Takintayo Akinbiyi, Mary Sara McPeek, Mark Abney

Abstract read
In one paragraph

Article in PLoS genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

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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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Takintayo AkinbiyiDepartment of Statistics, The University of Chicago, Chicago, Illinois, United States of America.
Mary Sara McPeekDepartment of Statistics, The University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0009-0007-7344-834X
Mark AbneyDepartment of Human Genetics, The University of Chicago, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0002-1718-5676

Funding

Methods for Human Genetic MappingR01HG001645 · NHGRI · UNIVERSITY OF CHICAGO · PI MCPEEK, MARY SARA · 2003 to 2023
$6.8M
NHGRI NIH HHS R01 HG001645
6 · The paper itself

Abstract

Understanding the genetic regulatory mechanisms of gene expression is an ongoing challenge. Genetic variants that are associated with expression levels are readily identified when they are proximal to the gene (i.e., cis-eQTLs), but SNPs distant from the gene whose expression levels they are associated with (i.e., trans-eQTLs) have been much more difficult to discover, even though they account for a majority of the heritability in gene expression levels. A major impediment to the identification of more trans-eQTLs is the lack of statistical methods that are powerful enough to overcome the obstacles of small effect sizes and large multiple testing burden of trans-eQTL mapping. Here, we propose ADELLE, a powerful statistical testing framework that requires only summary statistics and is designed to be most sensitive to SNPs that are associated with multiple gene expression levels, a characteristic of many trans-eQTLs. In simulations, we show that for detecting SNPs that are associated with 0.1%-2% of 10,000 traits, among the 8 methods we consider ADELLE is clearly the most powerful overall, with either the highest power or power not significantly different from the highest for all settings in that range. We apply ADELLE to a mouse advanced intercross line data set and show its ability to find trans-eQTLs that were not significant under a standard analysis. We also apply ADELLE to trans-eQTL mapping in the eQTLGen data, and for 1,451 previously identified trans-eQTLs, we discover trans association with additional expression traits beyond those previously identified. This demonstrates that ADELLE is a powerful tool at uncovering trans regulators of genetic expression.

Indexed as

Chromosome MappingQuantitative Trait LociAnimalsComputer SimulationGene Expression RegulationGenome-Wide Association StudyHumansMiceModels, GeneticPolymorphism, Single Nucleotide

Identifiers

PMID39792937
PMCPMC11756770

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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.