Evidence map›Paper›PMID 42730512›Full record

ArticleAnimal genetics2026

Towards a Standard Threshold for Genome Wide Significance in Dogs.

Mats E Pettersson, Katarina Tengvall, Jennifer R S Meadows

Abstract read
In one paragraph

Article in Animal genetics, 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

3 authors.

Mats E PetterssonDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-7372-9076
Katarina TengvallDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Jennifer R S MeadowsDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-0850-230X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide association studies (GWAS) are a foundational step in tying phenotype to genotype, relying on statistical significance thresholds to distinguish true- from false-positive signals of association. Dog genomics has long relied on per-study Bonferroni thresholds of significance, basing these on SNP chip levels of markers (~100 k to > 14 M variable sites). However, as the field progresses into whole genome imputation analyses and more powerful meta-analyses, there is a clear need to develop a standard significance threshold for common-variant GWAS. Using 1591 dogs from the broad-ancestry Dog10K dataset, we performed permutation analysis and developed GWAS thresholds for datasets using either 1% or 5% minor allele frequencies. The resultant p-values, 4.2 × 10

Indexed as

Genome-Wide Association StudyAnimalsBreedingDogsGene FrequencyGenotypeHaplotypesPhenotypePolymorphism, Single NucleotidedogGWASpermutationsignificance threshold

Identifiers

PMID42730512
PMCPMC13570322

What OpenQuestion 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 OpenQuestion graph.