Evidence map›Paper›PMID 26122927›Full record

ArticleGenetics, selection, evolution : GSE2015

Imputation of genotypes in Danish purebred and two-way crossbred pigs using low-density panels.

Tao Xiang, Peipei Ma, Tage Ostersen, Andres Legarra, Ole F Christensen

Abstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Tao XiangCenter for Quantitative Genetics and Genomics, Department of Molecular Biology and Genetics, Aarhus University, Tjele, DK-8830, Denmark. Tao.Xiang@mbg.au.dk.
Peipei MaCenter for Quantitative Genetics and Genomics, Department of Molecular Biology and Genetics, Aarhus University, Tjele, DK-8830, Denmark. Peipei.Ma@mbg.au.dk.
Tage OstersenPig Research Centre, Danish Agricultural and Food Council, Copenhagen, DK-1609, Denmark. TAO@seges.dk.
Andres LegarraINRA, UR1388 GenPhySE, CS-52627, Castanet-Tolosan, F-31326, France. Andres.Legarra@toulouse.inra.fr.
Ole F ChristensenCenter for Quantitative Genetics and Genomics, Department of Molecular Biology and Genetics, Aarhus University, Tjele, DK-8830, Denmark. OleF.Christensen@mbg.au.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenotype imputation is commonly used as an initial step in genomic selection since the accuracy of genomic selection does not decline if accurately imputed genotypes are used instead of actual genotypes but for a lower cost. Performance of imputation has rarely been investigated in crossbred animals and, in particular, in pigs. The extent and pattern of linkage disequilibrium differ in crossbred versus purebred animals, which may impact the performance of imputation. In this study, first we compared different scenarios of imputation from 5 K to 8 K single nucleotide polymorphisms (SNPs) in genotyped Danish Landrace and Yorkshire and crossbred Landrace-Yorkshire datasets and, second, we compared imputation from 8 K to 60 K SNPs in genotyped purebred and simulated crossbred datasets. All imputations were done using software Beagle version 3.3.2. Then, we investigated the reasons that could explain the differences observed.

resultsGenotype imputation performs as well in crossbred animals as in purebred animals when both parental breeds are included in the reference population. When the size of the reference population is very large, it is not necessary to use a reference population that combines the two breeds to impute the genotypes of purebred animals because a within-breed reference population can provide a very high level of imputation accuracy (correct rate ≥ 0.99, correlation ≥ 0.95). However, to ensure that similar imputation accuracies are obtained for crossbred animals, a reference population that combines both parental purebred animals is required. Imputation accuracies are higher when a larger proportion of haplotypes are shared between the reference population and the validation (imputed) populations.

conclusionsThe results from both real data and pedigree-based simulated data demonstrate that genotype imputation from low-density panels to medium-density panels is highly accurate in both purebred and crossbred pigs. In crossbred pigs, combining the parental purebred animals in the reference population is necessary to obtain high imputation accuracy.

Indexed as

GenotypeAnimalsInbreedingLinkage DisequilibriumModels, GeneticPolymorphism, Single NucleotidePopulation DensitySelection, GeneticSoftwareSwine

Identifiers

PMID26122927
PMCPMC4486706

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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.