Evidence map›Paper›PMID 39358442›Full record

ArticleScientific reports2024

Analyses of whole-genome sequences from 185 North American Thoroughbred horses, spanning 5 generations.

Ernie Bailey, Carrie J Finno, Jonah N Cullen, Ted Kalbfleisch, Jessica L Petersen

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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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

12 citing papers in PubMed.

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  8. Special Issue "Gene Doping Control".International journal of molecular sciences · 2026
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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

5 authors.

Ernie BaileyUniversity of Kentucky, Maxwell H. Gluck Equine Research Center, Lexington, KY, 40546, USA.
Carrie J FinnoUniversity of California-Davis, Population Health and Reproduction, Davis, CA, 95616, USA.
Jonah N CullenDepartment of Veterinary Population Medicine, University of Minnesota, St. Paul, MN, 55108, USA.
Ted KalbfleischUniversity of Kentucky, Maxwell H. Gluck Equine Research Center, Lexington, KY, 40546, USA. ted.kalbfleisch@uky.edu.
Jessica L PetersenDepartment of Animal Science, University of Nebraska-Lincoln, Lincoln, NE, 68583-0908, USA. jessica.petersen@unl.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole genome sequences (WGS) of 185 North American Thoroughbred horses were compared to quantify the number and frequency of variants, diversity of mitotypes, and autosomal runs of homozygosity (ROH). Of the samples, 82 horses were born between 1965 and 1986 (Group 1); the remaining 103, selected to maximize pedigree diversity, were born between 2000 and 2020 (Group 2). Over 14.3 million autosomal variants were identified with 4.5-5.0 million found per horse. Mitochondrial sequences associated the North American Thoroughbreds with 9 of 17 clades previously identified among diverse breeds. Individual coefficients of inbreeding, estimated from ROH, averaged 0.266 (Group 1) and 0.283 (Group 2). When SNP arrays were simulated using subsets of WGS markers, the arrays over-estimated lengths of ROH. WGS-based estimates of inbreeding were highly correlated (r > 0.98) with SNP array-based estimates, but only moderately correlated (r = 0.40) with inbreeding based on 5-generation pedigrees. On average, Group 1 horses had more heterozygous variants (P < 0.001), more total variants (P < 0.001), and lower individual inbreeding (F

Indexed as

HomozygoteInbreedingPedigreePolymorphism, Single NucleotideWhole Genome SequencingAnimalsBreedingFemaleGenetic VariationGenomeHorsesMaleNorth AmericaEquus caballusGenetic diversityInbreedingmtDNAPopulation geneticsVariant discovery

Identifiers

PMID39358442
PMCPMC11447028

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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.