Evidence map›Paper›PMID 32925905›Full record

ArticlePLoS genetics2020

Using prior information from humans to prioritize genes and gene-associated variants for complex traits in livestock.

Biaty Raymond, Loic Yengo, Roy Costilla, Chris Schrooten, Aniek C Bouwman, Ben J Hayes, Roel F Veerkamp, Peter M Visscher

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

9 citing papers in PubMed, 23 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Biaty RaymondAnimal Breeding and Genomics, Wageningen University and Research, Wageningen, The Netherlands.ORCID 0000-0003-1873-6764
Loic YengoInstitute for Molecular Bioscience, University of Queensland, St. Lucia, Australia.ORCID 0000-0002-4272-9305
Roy CostillaQueensland Alliance for Agriculture and Food Innovation, University of Queensland, St. Lucia, Australia.ORCID 0000-0003-0818-5065
Chris SchrootenCRV BV, Arnhem, The Netherlands.ORCID 0000-0002-0480-8416
Aniek C BouwmanAnimal Breeding and Genomics, Wageningen University and Research, Wageningen, The Netherlands.ORCID 0000-0001-5079-7108
Ben J HayesQueensland Alliance for Agriculture and Food Innovation, University of Queensland, St. Lucia, Australia.ORCID 0000-0002-5606-3970
Roel F VeerkampAnimal Breeding and Genomics, Wageningen University and Research, Wageningen, The Netherlands.ORCID 0000-0002-5240-6534
Peter M VisscherInstitute for Molecular Bioscience, University of Queensland, St. Lucia, Australia.
The University of Queensland · AUWageningen University & Research · NLCRV (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-Wide Association Studies (GWAS) in large human cohorts have identified thousands of loci associated with complex traits and diseases. For identifying the genes and gene-associated variants that underlie complex traits in livestock, especially where sample sizes are limiting, it may help to integrate the results of GWAS for equivalent traits in humans as prior information. In this study, we sought to investigate the usefulness of results from a GWAS on human height as prior information for identifying the genes and gene-associated variants that affect stature in cattle, using GWAS summary data on samples sizes of 700,000 and 58,265 for humans and cattle, respectively. Using Fisher's exact test, we observed a significant proportion of cattle stature-associated genes (30/77) that are also associated with human height (odds ratio = 5.1, p = 3.1e-10). Result of randomized sampling tests showed that cattle orthologs of human height-associated genes, hereafter referred to as candidate genes (C-genes), were more enriched for cattle stature GWAS signals than random samples of genes in the cattle genome (p = 0.01). Randomly sampled SNPs within the C-genes also tend to explain more genetic variance for cattle stature (up to 13.2%) than randomly sampled SNPs within random cattle genes (p = 0.09). The most significant SNPs from a cattle GWAS for stature within the C-genes did not explain more genetic variance for cattle stature than the most significant SNPs within random cattle genes (p = 0.87). Altogether, our findings support previous studies that suggest a similarity in the genetic regulation of height across mammalian species. However, with the availability of a powerful GWAS for stature that combined data from 8 cattle breeds, prior information from human-height GWAS does not seem to provide any additional benefit with respect to the identification of genes and gene-associated variants that affect stature in cattle.

Indexed as

AnimalsBody HeightBreedingCattleDatabases, GeneticGenetic VariationGenome-Wide Association StudyHumansLivestockMultifactorial InheritancePhenotypePolymorphism, Single NucleotideQuantitative Trait Loci

Identifiers

PMID32925905
PMCPMC7514049
OpenAlexW3084666299

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.