Evidence map›Paper›PMID 39922197›Full record

ArticleAmerican journal of human genetics2025

reg-eQTL: Integrating transcription factor effects to unveil regulatory variants.

Rekha Mudappathi, Tatiana Patton, Hai Chen, Ping Yang, Zhifu Sun, Panwen Wang, Chang-Xin Shi, Junwen Wang, Li Liu

Abstract read
In one paragraph

Article in American journal of human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

9 authors.

Rekha MudappathiCollege of Health Solutions, Arizona State University, Phoenix, AZ 85004, USA; Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA; Division of Epidemiology, Department of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, USA.
Tatiana PattonCollege of Health Solutions, Arizona State University, Phoenix, AZ 85004, USA; Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA.
Hai ChenCollege of Health Solutions, Arizona State University, Phoenix, AZ 85004, USA; Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA; Division of Epidemiology, Department of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, USA.
Ping YangDivision of Epidemiology, Department of Quantitative Health Sciences, Mayo Clinic, Scottsdale, AZ 85259, USA.
Zhifu SunDivision of Computational Biology, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA.
Panwen WangDepartment of Quantitative Health Sciences and Center for Individualized Medicine, Mayo Clinic, Scottsdale, AZ, USA.
Chang-Xin ShiDivision of Hematology/Oncology, Department of Medicine, Mayo Clinic, Scottsdale, AZ 85259, USA.
Junwen WangDepartment of Quantitative Health Sciences and Center for Individualized Medicine, Mayo Clinic, Scottsdale, AZ, USA; Division of Applied Oral Sciences & Community Dental Care, Faculty of Dentistry, The University of Hong Kong, 34 Hospital Road, Hong Kong SAR, China.
Li LiuCollege of Health Solutions, Arizona State University, Phoenix, AZ 85004, USA; Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA. Electronic address: liliu@asu.edu.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
Discover and Analyze Germline-Somatic Interactions in CancerR01LM013438 · NLM · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI LIU, LI, YANG, PING · 2021 to 2023
$1.0M
NCI NIH HHS P30 CA015083NLM NIH HHS R01 LM013438
6 · The paper itself

Abstract

Regulatory single-nucleotide variants (rSNVs) in noncoding regions of the genome play a crucial role in gene transcription by altering transcription factor (TF) binding, chromatin states, and other epigenetic modifications. Existing expression quantitative trait locus (eQTL) methods identify genomic loci associated with gene-expression changes, but they often fall short in pinpointing causal variants. We introduce reg-eQTL, a computational method that incorporates TF effects and interactions with genetic variants into eQTL analysis. This approach provides deeper insights into the regulatory mechanisms, bringing us one step closer to identifying potential causal variants by uncovering how TFs interact with SNVs to influence gene expression. This method defines a trio consisting of a genetic variant, a target gene, and a TF and tests its impact on gene transcription. In comprehensive simulations, reg-eQTL shows improved power of detecting rSNVs with low population frequency, weak effects, and synergetic interaction with TF as compared to traditional eQTL methods. Application of reg-eQTL to GTEx data from lung, brain, and whole-blood tissues uncovered regulatory trios that include eQTLs and increased the number of eQTLs shared across tissue types. Regulatory networks constructed on the basis of these trios reveal intricate gene regulation across tissue types.

Indexed as

Polymorphism, Single NucleotideQuantitative Trait LociTranscription FactorsComputational BiologyGene Expression RegulationGene Regulatory NetworksGenome-Wide Association StudyHumansTranscription FactorsbioinformaticseQTL analysisrare SNVsregulatory triosTF-SNV interactiontissue-specific eQTLstranscription factors

Identifiers

PMID39922197
PMCPMC11947170

What Socratic holds

Textmetadata
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 Socratic graph.