Evidence map›Paper›PMID 31467030›Full record

ArticleG3 (Bethesda, Md.)2019

Genomic Prediction Including SNP-Specific Variance Predictors.

Elena Flavia Mouresan, Maria Selle, Lars Rönnegård

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

The trial behind it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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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

3 authors.

Elena Flavia MouresanDepartment of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Sweden, 75007, elena.flavia.mouresan@slu.se.ORCID 0000-0002-1335-7610
Maria SelleDepartment of Mathematical Sciences, Norwegian University of Science and Technology, Norway, 7491, and.ORCID 0000-0002-2062-3235
Lars RönnegårdDepartment of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Sweden, 75007.ORCID 0000-0002-1057-5401

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing amount of available biological information on the markers can be used to inform the models applied for genomic selection to improve predictions. The objective of this study was to propose a general model for genomic selection using a link function approach within the hierarchical generalized linear model framework (hglm) that can include external information on the markers. These models can be fitted using the well-established hglm package in R. We also present an R package (CodataGS) to fit these models, which is significantly faster than the hglm package. Simulated data were used to validate the proposed model. We tested categorical, continuous and combination models where the external information on the markers was related to 1) the location of the QTL on the genome with varying degree of uncertainty, 2) the relationship of the markers with the QTL calculated as the LD between them, and 3) a combination of both. The proposed models showed improved accuracies from 3.8% up to 23.2% compared to the SNP-BLUP method in a simulated population derived from a base population with 100 individuals. Moreover, the proposed categorical model was tested on a dairy cattle dataset for two traits (Milk Yield and Fat Percentage). These results also showed improved accuracy compared to SNP-BLUP, especially for the Fat% trait. The performance of the proposed models depended on the genetic architecture of the trait, as traits that deviate from the infinitesimal model benefited more from the external information. Also, the gain in accuracy depended on the degree of uncertainty of the external information provided to the model. The usefulness of these type of models is expected to increase with time as more accurate information on the markers becomes available.

Indexed as

GenomePolymorphism, Single NucleotideAlgorithmsAnimalsCattleComputational BiologyEvolution, MolecularGenetics, PopulationGenomicsModels, GeneticQuantitative Trait LociBLUPCodataGSexternal informationGenomic PredictionGenPredhglmShared Data Resources

Identifiers

PMID31467030
PMCPMC6778789

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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.