Evidence map›Paper›PMID 28093063›Full record

ArticleGenetics, selection, evolution : GSE2017

Whole-genome sequence-based genomic prediction in laying chickens with different genomic relationship matrices to account for genetic architecture.

Guiyan Ni, David Cavero, Anna Fangmann, Malena Erbe, Henner Simianer

Abstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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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3 · Its place in the literature

Who cites it

35 citing papers in PubMed.

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  10. Genomic selection in tropical perennial crops and plantation trees: a review.Molecular breeding : new strategies in plant improvement · 2022
    Review
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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.

Guiyan NiAnimal Breeding and Genetics Group, Georg-August-Universität, Göttingen, Germany. gyni.ni@agr.uni-goettingen.de.
David CaveroLohmann Tierzucht GmbH, Cuxhaven, Germany.
Anna FangmannAnimal Breeding and Genetics Group, Georg-August-Universität, Göttingen, Germany.
Malena ErbeAnimal Breeding and Genetics Group, Georg-August-Universität, Göttingen, Germany.
Henner SimianerAnimal Breeding and Genetics Group, Georg-August-Universität, Göttingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWith the availability of next-generation sequencing technologies, genomic prediction based on whole-genome sequencing (WGS) data is now feasible in animal breeding schemes and was expected to lead to higher predictive ability, since such data may contain all genomic variants including causal mutations. Our objective was to compare prediction ability with high-density (HD) array data and WGS data in a commercial brown layer line with genomic best linear unbiased prediction (GBLUP) models using various approaches to weight single nucleotide polymorphisms (SNPs).

methodsA total of 892 chickens from a commercial brown layer line were genotyped with 336 K segregating SNPs (array data) that included 157 K genic SNPs (i.e. SNPs in or around a gene). For these individuals, genome-wide sequence information was imputed based on data from re-sequencing runs of 25 individuals, leading to 5.2 million (M) imputed SNPs (WGS data), including 2.6 M genic SNPs. De-regressed proofs (DRP) for eggshell strength, feed intake and laying rate were used as quasi-phenotypic data in genomic prediction analyses. Four weighting factors for building a trait-specific genomic relationship matrix were investigated: identical weights, -(log

resultsAveraged over the three traits, the highest predictive ability (0.366 ± 0.075) was obtained when only genic SNPs from WGS data were used. Predictive abilities with genic SNPs and all SNPs from HD array data were 0.361 ± 0.072 and 0.353 ± 0.074, respectively. Prediction with -(log

conclusionsOur results show that little or no benefit was gained when using all imputed WGS data to perform genomic prediction compared to using HD array data regardless of the weighting factors tested. However, using only genic SNPs from WGS data had a positive effect on prediction ability.

Indexed as

GenomeGenomicsModels, GeneticAlgorithmsAllelesAnimalsBreedingChickensChromosome MappingFemaleGenome-Wide Association StudyHigh-Throughput Nucleotide SequencingMaleOligonucleotide Array Sequence AnalysisPolymorphism, Single Nucleotide

Identifiers

PMID28093063
PMCPMC5238523

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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.