Evidence map›Paper›PMID 40121435›Full record

ArticleBMC genomics2025

Multi-tool copy number detection highlights common body size-associated variants in miniature pig breeds from different geographical regions.

Jan Berghöfer, Nadia Khaveh, Stefan Mundlos, Julia Metzger

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Convergence and Parallelism of Phenotypic and Molecular Genetic Variability in Some Species.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2026
    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

4 authors.

Jan BerghöferMax Planck Institute for Molecular Genetics, Berlin, Germany.
Nadia KhavehMax Planck Institute for Molecular Genetics, Berlin, Germany.
Stefan MundlosMax Planck Institute for Molecular Genetics, Berlin, Germany.
Julia MetzgerMax Planck Institute for Molecular Genetics, Berlin, Germany. julia.metzger@tiho-hannover.de.

Funding

Deutsche Forschungsgemeinschaft ME4517/3-1Deutsche Forschungsgemeinschaft ME4517/4-1
6 · The paper itself

Abstract

backgroundCopy number variations (CNVs) represent a common and highly specific type of variation in the genome, potentially influencing genetic diversity and mammalian phenotypic development. Structural variants, such as deletions, duplications, and insertions, have frequently been highlighted as key factors influencing traits in high-production pigs. However, comprehensive CNV analyses in miniature pig breeds are limited despite their value in biomedical research.

resultsThis study performed whole-genome sequencing in 36 miniature pigs from nine breeds from America, Asia and Oceania, and Europe. By employing a multi-tool approach (CNVpytor, Delly, GATK gCNV, Smoove), the accuracy of CNV identification was improved. In total, 34 homozygous CNVs overlapped with exonic regions in all samples, suggesting a role in expressing specific phenotypes such as uniform growth patterns, fertility, or metabolic function. In addition, 386 copy number variation regions (CNVRs) shared by all breeds were detected, covering 33.6 Mb (1.48% of the autosomal genome). Further, 132 exclusive CNVRs were identified for American breeds, 47 for Asian and Oceanian breeds, and 114 for European breeds. Functional enrichment analysis revealed genes within the common CNVRs involved in body height determination and other growth-related parameters. Exclusive CNVRs were located in the region of genes enriched for lipid metabolism in American minipigs, reproductive traits in Asian and Oceanian breeds, and cardiovascular features and body height in European breeds. In the selected groups, quantitative trait loci associated with body size, meat quality, reproduction, and disease susceptibility were highlighted.

conclusionThis investigation of the CNV landscape of minipigs underlines the impact of selective breeding on structural variants and its role in the development of specific breed phenotypes across geographical areas. The multi-tool approach provides a valuable resource for future studies on the effects of artificial selection on livestock genomes.

Indexed as

Body SizeDNA Copy Number VariationsSwine, MiniatureAnimalsBreedingGeographyPhenotypeQuantitative Trait LociSwineWhole Genome SequencingBiomedical researchCopy number variationFunctional enrichmentGenetic diversityMiniature pigsNext-generation sequencingPig genomeQuantitative trait lociRegional adaptation

Identifiers

PMID40121435
PMCPMC11929999

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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.