Evidence map›Paper›PMID 30795734›Full record

ArticleBMC genetics2019

Increasing accuracy of genomic selection in presence of high density marker panels through the prioritization of relevant polymorphisms.

Ling-Yun Chang, Sajjad Toghiani, Samuel E Aggrey, Romdhane Rekaya

Abstract read
In one paragraph

Article in BMC genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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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

12 citing papers in PubMed.

  1. Article
  2. Review
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  6. FGenes · 2025
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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

4 authors.

Ling-Yun ChangDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA. Ling-Yun.Chang@genusplc.com.ORCID 0000-0002-2000-4274
Sajjad ToghianiDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.
Samuel E AggreyDepartment of Poultry Science, University of Georgia, Athens, GA, 30602, USA.
Romdhane RekayaDepartment of Animal and Dairy Science, University of Georgia, Athens, GA, 30602, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt becomes clear that the increase in the density of marker panels and even the use of sequence data didn't result in any meaningful increase in the accuracy of genomic selection (GS) using either regression (RM) or variance component (VC) approaches. This is in part due to the limitations of current methods. Association model are well over-parameterized and suffer from severe co-linearity and lack of statistical power. Even when the variant effects are not directly estimated using VC based approaches, the genomic relationships didn't improve after the marker density exceeded a certain threshold. SNP prioritization-based fixation index (F

resultsTwo populations with average LD between adjacent markers of 0.3 (P1) and 0.7 (P2) were simulated. In both populations, the genomic data consisted of 400 K SNP markers distributed on 10 chromosomes. The density of simulated genomic data mimics roughly 1.2 million SNP markers in the bovine genome. The genomic relationship matrix (G) was calculated for each set of selected SNPs based on their F

conclusionsGenomic similarity could be maximized by the decrease in the number of selected SNPs, but it also leads to a decrease in the percentage of genetic variation explained by the selected markers. Finding the balance between these two parameters could optimize the accuracy of GS in the presence of high density marker panels.

Indexed as

BreedingGenomicsPolymorphism, GeneticAnimalsBody WeightGenetic MarkersLinkage DisequilibriumLivestockPolymorphism, Single NucleotideQuantitative Trait LociWeaningGenetic MarkersGenomic selectionHigh density panelSNP prioritization

Identifiers

PMID30795734
PMCPMC6387489

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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.