Evidence map›Paper›PMID 42282660›Full record

ArticlebioRxiv : the preprint server for biology2026

An interpretable machine learning framework for dog breed inference and ancestry decomposition.

Yiming Bian, Rob Bierman, Noah Snyder-Mackler, Daniel Promislow, Elinor Karlsson, Dog Aging Project Consortium, Joshua M Akey

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

7 authors.

Yiming BianLewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, South Drive, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-8725-3603
Rob BiermanLewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, South Drive, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0001-8513-7425
Noah Snyder-MacklerCenter for Evolution & Medicine, Arizona State University; Tempe, AZ 85251, USA.ORCID 0000-0003-3026-6160
Daniel PromislowJean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA.ORCID 0000-0001-7088-4495
Elinor KarlssonGenomics & Computational Biology, UMass Chan Medical School; Worcester, MA 01655, USA.ORCID 0000-0002-4343-3776
Dog Aging Project Consortium
Joshua M AkeyLewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, South Drive, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-4411-1330

Funding

The Dog Aging Project: Genetic and Environmental Determinants of Healthy Aging in Companion Dogs Competitive RevisionU19AG057377 · NIA · UNIVERSITY OF WASHINGTON · PI PROMISLOW, DANIEL EDWARD · 2018 to 2023
$29.0M
NIA NIH HHS U19 AG057377
6 · The paper itself

Abstract

The over 300 currently recognized breeds of domesticated dogs are the culmination of centuries of intense artificial selection and recurrent population bottlenecks. While breed labels are widely used in genetic and veterinary studies, inferring breed identity from genomic data remains challenging due to the high dimensionality of genotype data, uneven sampling across breeds, and admixture resulting in mixed-breed individuals. Here, we present an interpretable machine learning framework to infer dog breed labels from genome-wide SNP data. Our approach combines dimensionality reduction with a multi-output random forest model that maps genetic variation to a continuous representation of breed membership, enabling both classification and mixed-breed inference. We apply this framework to the Dog Aging Project (DAP) dataset of 6,572 purebred and mixed-breed dogs across 100 breed classes, achieving 91.7% accuracy with an overlap-based metric, outperforming an ADMIXTURE-based benchmark that achieved 87.8% accuracy. Notably, we find that as few as 150 informative SNPs are sufficient to achieve near-maximal predictive performance, highlighting the highly structured nature of canine genetic variation. We also introduce a SNP importance score metric that links model predictions back to individual genetic variants. Analysis of top-ranked variants reveals loci previously associated with morphological, pigmentation, and behavioral traits, as well as candidate loci lacking prior phenotypic annotation, supporting both the biological relevance and discovery potential of the framework. Together, these results demonstrate that our framework provides an accurate, flexible, and interpretable approach to predict breed ancestry, with applications in veterinary genomics, canine population genetics, and the identification of loci underlying hallmark breed phenotypes.

Identifiers

PMID42282660
PMCPMC13252084

What Socratic 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 Socratic graph.