Evidence map›Paper›PMID 42202282›Full record

ArticleBriefings in bioinformatics2026

ceQTL: a co-expression QTL model to detect a variant that affects transcription factor binding and its target regulation.

Panwen Wang, Yanxi Chen, Yong Liu, Li Liu, Ping Yang, Junwen Wang, Zhifu Sun

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Panwen WangDepartment of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, United States.
Yanxi ChenDepartment of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, United States.
Yong LiuDepartment of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, United States.
Li LiuCollege of Health Solutions, Arizona State University, Phoenix, AZ 85004, United States.ORCID 0000-0003-4002-7497
Ping YangDepartment of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, United States.ORCID 0000-0002-8588-847X
Junwen WangDepartment of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, United States.ORCID 0000-0002-4432-4707
Zhifu SunDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expression quantitative trait locus (eQTL) mapping is used to identify the functional link between a genomic variant and a gene's expression. A significant eQTL association does not mean a causal relationship or mechanism, and further investigation is needed to understand how a single-nucleotide polymorphism (SNP) impacts gene expression. One of the most plausible explanations for eQTL is that a genomic variant affects transcription factor (TF) binding and thus impacts its regulation on target genes (TGs). However, the current eQTL model does not provide information on the TF and how its regulation is mediated by the SNP's genotypes. Here, we propose a new method called differential co-expression QTL (ceQTL) among different alleles using Chow statistics to specifically detect eQTLs that are bound by a particular TF. We start with building a trio of TF, its TG, and related SNP, and then test the significant coefficient difference among different genotypes of the SNP. We applied this ceQTL model to simulated data and the lung tissue datasets from the genotype-tissue expression project. The simulated data results showed that the model was robust to detect true ceQTLs at variable sample sizes and different minor allele frequencies as measured by area under the curve. Our tool also performed a TF binding affinity analysis to add another layer of evidence for functional interpretation. In summary, ceQTL analysis provides a more interpretable and biological insight into the mechanism of eQTL and transcriptomic regulation, which would help us better understand how genomic variants affect phenotypes and diseases.

Indexed as

Gene Expression RegulationModels, GeneticPolymorphism, Single NucleotideQuantitative Trait LociTranscription FactorsAllelesGenotypeHumansProtein BindingTranscription FactorsceQTLdifferential co-expression QTLeQTLexpression quantitative trait locusgene expression regulationGTEx projectsingle nucleotide polymorphismSNPtranscription factor

Identifiers

PMID42202282
PMCPMC13215588

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.