Evidence map›Paper›PMID 41908915›Full record

ArticleGigaByte (Hong Kong, China)2026

Inference of admixture in dogs from whole genome sequences.

Gregory Kislik, Garrett Moore, Liudmilla Rubbi, Veninka Nikki Supara, Grace Chen, Matteo Pellegrini

Abstract read
In one paragraph

Article in GigaByte (Hong Kong, China), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Gregory KislikMolecular Cell and Developmental Biology, University of California, Los Angeles (UCLA), CA, Los Angeles, USA.ORCID https://orcid.org/0009-0003-2741-3892
Garrett MooreProsper DNA, Los Angeles, CA, USA.
Liudmilla RubbiMolecular Cell and Developmental Biology, University of California, Los Angeles (UCLA), CA, Los Angeles, USA.
Veninka Nikki SuparaMolecular Cell and Developmental Biology, University of California, Los Angeles (UCLA), CA, Los Angeles, USA.
Grace ChenMolecular Cell and Developmental Biology, University of California, Los Angeles (UCLA), CA, Los Angeles, USA.
Matteo PellegriniMolecular Cell and Developmental Biology, University of California, Los Angeles (UCLA), CA, Los Angeles, USA.ORCID https://orcid.org/0000-0003-0867-5398

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Understanding the genetic architecture of domestic dogs provides unique insights into the processes of domestication, breed formation, and the genetic basis of complex traits and diseases. Dog populations, characterized by their diverse morphologies and behaviors, also exhibit extensive evidence of historical and ongoing admixture. This widespread mixing, driven by both natural migration and selective breeding practices, has profoundly shaped the genomic landscape of modern dog breeds. Though global admixture has been extensively estimated in human population studies, where the number of subgroups is typically limited, there has been more limited analysis in canines, where there may be dozens of ancestral groups, or breeds. Results: Here we present a procedure for estimating global admixture in dogs from whole genome sequence data using SCOPE. We created a reference population of 65 dog breeds that included 349 individuals, from which we determined breed-informative SNPs. We demonstrate that SCOPE can accurately infer breed composition in both simulated and real admixed samples, even at low sequencing depths. We also characterized the genetic similarity between our reference dog breeds and recovered previously reported relationships. Conclusion: This approach allows us to identify the strength of the genetic signature of breeds and place error bounds on admixture estimates. It also provides evidence that admixture can be accurately inferred in subjects that may originate from multiple ancestral populations.

Identifiers

PMID41908915
PMCPMC13022507

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.