Evidence map›Paper›PMID 40999335›Full record

ArticleGenetics, selection, evolution : GSE2025

Effect of using preselected markers from imputed whole-genome sequence for genomic prediction in Angus cattle.

Nantapong Kamprasert, Hassan Aliloo, Julius H J van der Werf, Christian J Duff, Samuel A Clark

Abstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 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

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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Genome-Wide Development and Validation of KASP-Based SNP Markers inAnimals : an open access journal from MDPI · 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

5 authors.

Nantapong KamprasertSchool of Environmental and Rural Science, University of New England, Armidale, NSW, 2351, Australia. nkampras@myune.edu.au.ORCID http://orcid.org/0000-0001-5747-7043
Hassan AlilooSchool of Environmental and Rural Science, University of New England, Armidale, NSW, 2351, Australia.
Julius H J van der WerfSchool of Environmental and Rural Science, University of New England, Armidale, NSW, 2351, Australia.
Christian J DuffAngus Australia, Glen Innes Road, Armidale, NSW, 2350, Australia.
Samuel A ClarkSchool of Environmental and Rural Science, University of New England, Armidale, NSW, 2351, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe advent of next-generation sequencing enables the opportunity to use denser marker tools, up to whole-genome sequences (WGS), for genomic prediction in livestock. Improvement in genomic prediction (GP) accuracy from using WGS has been observed in simulation studies. In contrast, such advantage has found to be inconsistent once implemented in practice. The benefit of WGS appears to be from markers that are significant for the trait of interest. Thus, the main objective of this study was to investigate the predictive ability of adding preselected markers to the standard-industry 50k genotype for GP of economically important traits in Angus cattle, namely, birth weight (BW), scrotal circumference (SC), carcass weight (CWT) and carcass intramuscular fat (CIMF). Animals were genotyped with either commercial or customised SNP-genotyping arrays; then, the genotypes were imputed to WGS. The 50k genotype was used as the control group. Informative markers associated with the desired traits were extracted from WGS, then were added to the 50k genotype. Several methods were chosen to select different sets of informative markers, including LD-based pruning, top SNP from a genome-wide association study (GWAS), functional annotation based on Gene Ontology, cattle QTL database, and sequence annotation. In total, eight different sets of genotypes were investigated. We applied different statistical models to predict genomic breeding values, including GBLUP, BayesR, and BayesRC, and two-GRM GBLUP constructed separately from the 50k and the preselected genotype set.

resultsHeritability (h

conclusionsThe findings suggest that potential improvements may be achieved by using preselected SNPs from the GWAS, a method that has proven within the population. The performance of preselected markers on GP influenced by several factors, including population structure, method used to select significant markers, and genetic architecture of traits.

Indexed as

GenomicsWhole Genome SequencingAnimalsBreedingCattleGenetic MarkersGenomeGenome-Wide Association StudyGenotypeMaleModels, GeneticPhenotypePolymorphism, Single NucleotideQuantitative Trait LociGenetic Markers

Identifiers

PMID40999335
PMCPMC12465657

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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.