Evidence map›Paper›PMID 32050893›Full record

ArticleGenetics, selection, evolution : GSE2020

Beyond large-effect loci: large-scale GWAS reveals a mixed large-effect and polygenic architecture for age at maturity of Atlantic salmon.

Marion Sinclair-Waters, Jørgen Ødegård, Sven Arild Korsvoll, Thomas Moen, Sigbjørn Lien, Craig R Primmer, Nicola J Barson

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
12.8field-weighted citation impact, top 1% of its field
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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

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  20. A complex mechanism translating variation of a simple genetic architecture into alternative life histories.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

7 authors at 3 institutions in 2 countries.

Marion Sinclair-WatersOrganismal and Evolutionary Biology Research Programme, University of Helsinki, Helsinki, Finland. msinclairwaters@gmail.com.ORCID http://orcid.org/0000-0001-7371-4547
Jørgen ØdegårdAquaGen, Trondheim, Norway.
Sven Arild KorsvollAquaGen, Trondheim, Norway.
Thomas MoenAquaGen, Trondheim, Norway.
Sigbjørn LienCentre for Integrative Genetics, Department of Animal and Aquacultural Sciences, Faculty of Biosciences, Norwegian University of Life Sciences, Ås, Norway.
Craig R PrimmerOrganismal and Evolutionary Biology Research Programme, University of Helsinki, Helsinki, Finland.
Nicola J BarsonCentre for Integrative Genetics, Department of Animal and Aquacultural Sciences, Faculty of Biosciences, Norwegian University of Life Sciences, Ås, Norway.
AquaGen (Norway) · NONorwegian University of Life Sciences · NOUniversity of Helsinki · FI

Funding

Academy of Finland 302873Academy of Finland 307593Research Council of Norway 254852 - QuantEscape2
6 · The paper itself

Abstract

backgroundUnderstanding genetic architecture is essential for determining how traits will change in response to evolutionary processes such as selection, genetic drift and/or gene flow. In Atlantic salmon, age at maturity is an important life history trait that affects factors such as survival, reproductive success, and growth. Furthermore, age at maturity can seriously impact aquaculture production. Therefore, characterizing the genetic architecture that underlies variation in age at maturity is of key interest.

resultsHere, we refine our understanding of the genetic architecture for age at maturity of male Atlantic salmon using a genome-wide association study of 11,166 males from a single aquaculture strain, using imputed genotypes at 512,397 single nucleotide polymorphisms (SNPs). All individuals were genotyped with a 50K SNP array and imputed to higher density using parents genotyped with a 930K SNP array and pedigree information. We found significant association signals on 28 of 29 chromosomes (P-values: 8.7 × 10 DISCUSSION: These results reveal a mixed architecture of large-effect loci and a polygenic component that consists of multiple smaller-effect loci, suggesting a more complex genetic architecture of Atlantic salmon age at maturity than previously thought. This more complex architecture will have implications for selection on this key trait in aquaculture and for management of wild salmon populations.

Indexed as

Genome-Wide Association StudyMultifactorial InheritanceAnimalsAquacultureBiological EvolutionBreedingChromosomesFemaleGenotypeMalePhenotypePolymorphism, Single NucleotideSalmo salar

Identifiers

PMID32050893
PMCPMC7017552
OpenAlexW3005673236

What OpenQuestion holds

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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 OpenQuestion graph.