Evidence map›Paper›PMID 42497061›Full record

ArticleSTAR protocols2026

Protocol for detecting causal variants by co-localizing GWAS and QTL studies using colocRedRibbon.

Theodora Papadopoulou, Aristeidis Sionakidis, Anthony Piron, Miriam Cnop

Abstract read
In one paragraph

Article in STAR protocols, 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

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.

Theodora PapadopoulouULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, 1070 Brussels, Belgium; Interuniversity Institute of Bioinformatics in Brussels (IB2), 1050 Brussels, Belgium. Electronic address: theodora.papadopoulou@ulb.be.
Aristeidis SionakidisPrecision Breast Cancer Institute, Department of Oncology, University of Cambridge, Cambridge CB2 0QQ, UK.
Anthony PironInteruniversity Institute of Bioinformatics in Brussels (IB2), 1050 Brussels, Belgium; Pharmacognosy, Bioanalysis and Drug Discovery, Pharmacy Faculty, Université Libre de Bruxelles, 1050 Brussels, Belgium. Electronic address: anthony.piron@ulb.be.
Miriam CnopULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles, 1070 Brussels, Belgium; Department of Endocrinology, ULB Erasmus Hospital, Brussels University Hospital, Université Libre de Bruxelles, 1070 Brussels, Belgium; WEL Research Institute, 1300 Wavre, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we present a protocol for using colocRedRibbon to link disease-associated variants to gene expression variation by co-localizing genome-wide association study (GWAS) SNPs with cis-expression quantitative trait loci (eQTLs). We describe steps for shortlisting GWAS and eQTL variants, computing co-localization statistics, and assessing posterior probabilities. Co-localized variants provide insights into disease mechanisms and potential therapeutic targets. Beyond GWAS-eQTL integration, the protocol can be applied to co-localization analyses across different QTL types and distinct GWAS datasets. For complete details on the use and execution of this protocol, please refer to Piron et al.

Indexed as

BioinformaticsGenomicsHealth SciencesHigh Throughput Screening

Identifiers

PMID42497061
PMCPMC13427430

What OpenQuestion holds

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Registered trials

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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.