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The utility of low-density genotyping for imputation in the Thoroughbred horse

BACKGROUND: Despite the dramatic reduction in the cost of high-density genotyping that has occurred over the last decade, it remains one of the limiting factors for obtaining the large datasets required for genomic studies of disease in the horse. In this study, we investigated the potential for low...

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Autores principales: Corbin, Laura J, Kranis, Andreas, Blott, Sarah C, Swinburne, June E, Vaudin, Mark, Bishop, Stephen C, Woolliams, John A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930001/
https://www.ncbi.nlm.nih.gov/pubmed/24495673
http://dx.doi.org/10.1186/1297-9686-46-9
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author Corbin, Laura J
Kranis, Andreas
Blott, Sarah C
Swinburne, June E
Vaudin, Mark
Bishop, Stephen C
Woolliams, John A
author_facet Corbin, Laura J
Kranis, Andreas
Blott, Sarah C
Swinburne, June E
Vaudin, Mark
Bishop, Stephen C
Woolliams, John A
author_sort Corbin, Laura J
collection PubMed
description BACKGROUND: Despite the dramatic reduction in the cost of high-density genotyping that has occurred over the last decade, it remains one of the limiting factors for obtaining the large datasets required for genomic studies of disease in the horse. In this study, we investigated the potential for low-density genotyping and subsequent imputation to address this problem. RESULTS: Using the haplotype phasing and imputation program, BEAGLE, it is possible to impute genotypes from low- to high-density (50K) in the Thoroughbred horse with reasonable to high accuracy. Analysis of the sources of variation in imputation accuracy revealed dependence both on the minor allele frequency of the single nucleotide polymorphisms (SNPs) being imputed and on the underlying linkage disequilibrium structure. Whereas equidistant spacing of the SNPs on the low-density panel worked well, optimising SNP selection to increase their minor allele frequency was advantageous, even when the panel was subsequently used in a population of different geographical origin. Replacing base pair position with linkage disequilibrium map distance reduced the variation in imputation accuracy across SNPs. Whereas a 1K SNP panel was generally sufficient to ensure that more than 80% of genotypes were correctly imputed, other studies suggest that a 2K to 3K panel is more efficient to minimize the subsequent loss of accuracy in genomic prediction analyses. The relationship between accuracy and genotyping costs for the different low-density panels, suggests that a 2K SNP panel would represent good value for money. CONCLUSIONS: Low-density genotyping with a 2K SNP panel followed by imputation provides a compromise between cost and accuracy that could promote more widespread genotyping, and hence the use of genomic information in horses. In addition to offering a low cost alternative to high-density genotyping, imputation provides a means to combine datasets from different genotyping platforms, which is becoming necessary since researchers are starting to use the recently developed equine 70K SNP chip. However, more work is needed to evaluate the impact of between-breed differences on imputation accuracy.
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spelling pubmed-39300012014-03-04 The utility of low-density genotyping for imputation in the Thoroughbred horse Corbin, Laura J Kranis, Andreas Blott, Sarah C Swinburne, June E Vaudin, Mark Bishop, Stephen C Woolliams, John A Genet Sel Evol Research BACKGROUND: Despite the dramatic reduction in the cost of high-density genotyping that has occurred over the last decade, it remains one of the limiting factors for obtaining the large datasets required for genomic studies of disease in the horse. In this study, we investigated the potential for low-density genotyping and subsequent imputation to address this problem. RESULTS: Using the haplotype phasing and imputation program, BEAGLE, it is possible to impute genotypes from low- to high-density (50K) in the Thoroughbred horse with reasonable to high accuracy. Analysis of the sources of variation in imputation accuracy revealed dependence both on the minor allele frequency of the single nucleotide polymorphisms (SNPs) being imputed and on the underlying linkage disequilibrium structure. Whereas equidistant spacing of the SNPs on the low-density panel worked well, optimising SNP selection to increase their minor allele frequency was advantageous, even when the panel was subsequently used in a population of different geographical origin. Replacing base pair position with linkage disequilibrium map distance reduced the variation in imputation accuracy across SNPs. Whereas a 1K SNP panel was generally sufficient to ensure that more than 80% of genotypes were correctly imputed, other studies suggest that a 2K to 3K panel is more efficient to minimize the subsequent loss of accuracy in genomic prediction analyses. The relationship between accuracy and genotyping costs for the different low-density panels, suggests that a 2K SNP panel would represent good value for money. CONCLUSIONS: Low-density genotyping with a 2K SNP panel followed by imputation provides a compromise between cost and accuracy that could promote more widespread genotyping, and hence the use of genomic information in horses. In addition to offering a low cost alternative to high-density genotyping, imputation provides a means to combine datasets from different genotyping platforms, which is becoming necessary since researchers are starting to use the recently developed equine 70K SNP chip. However, more work is needed to evaluate the impact of between-breed differences on imputation accuracy. BioMed Central 2014-02-04 /pmc/articles/PMC3930001/ /pubmed/24495673 http://dx.doi.org/10.1186/1297-9686-46-9 Text en Copyright © 2014 Corbin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Corbin, Laura J
Kranis, Andreas
Blott, Sarah C
Swinburne, June E
Vaudin, Mark
Bishop, Stephen C
Woolliams, John A
The utility of low-density genotyping for imputation in the Thoroughbred horse
title The utility of low-density genotyping for imputation in the Thoroughbred horse
title_full The utility of low-density genotyping for imputation in the Thoroughbred horse
title_fullStr The utility of low-density genotyping for imputation in the Thoroughbred horse
title_full_unstemmed The utility of low-density genotyping for imputation in the Thoroughbred horse
title_short The utility of low-density genotyping for imputation in the Thoroughbred horse
title_sort utility of low-density genotyping for imputation in the thoroughbred horse
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930001/
https://www.ncbi.nlm.nih.gov/pubmed/24495673
http://dx.doi.org/10.1186/1297-9686-46-9
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