Using genomic relationship likelihood for parentage assignment

Abstract Background Parentage assignment is usually based on a limited number of unlinked, independent genomic markers (microsatellites, low-density single nucleotide polymorphisms (SNPs), etc.). Classical methods for parentage assignment are exclusion-based (i.e. based on loci that violate Mendelia...

Full description

Bibliographic Details
Main Authors: Kim E. Grashei, Jørgen Ødegård, Theo H. E. Meuwissen
Format: Article
Language:deu
Published: BMC 2018-05-01
Series:Genetics Selection Evolution
Online Access:http://link.springer.com/article/10.1186/s12711-018-0397-7
id doaj-87f6931161644c8892f0c0d3a1b84072
record_format Article
spelling doaj-87f6931161644c8892f0c0d3a1b840722020-11-25T00:43:12ZdeuBMCGenetics Selection Evolution1297-96862018-05-0150111110.1186/s12711-018-0397-7Using genomic relationship likelihood for parentage assignmentKim E. Grashei0Jørgen Ødegård1Theo H. E. Meuwissen2AquaGen ASAquaGen ASDepartment of Animal and Aquacultural Sciences, Norwegian University of Life SciencesAbstract Background Parentage assignment is usually based on a limited number of unlinked, independent genomic markers (microsatellites, low-density single nucleotide polymorphisms (SNPs), etc.). Classical methods for parentage assignment are exclusion-based (i.e. based on loci that violate Mendelian inheritance) or likelihood-based, assuming independent inheritance of loci. For true parent–offspring relations, genotyping errors cause apparent violations of Mendelian inheritance. Thus, the maximum proportion of such violations must be determined, which is complicated by variable call- and genotype error rates among loci and individuals. Recently, genotyping using high-density SNP chips has become available at lower cost and is increasingly used in genetics research and breeding programs. However, dense SNPs are not independently inherited, violating the assumptions of the likelihood-based methods. Hence, parentage assignment usually assumes a maximum proportion of exclusions, or applies likelihood-based methods on a smaller subset of independent markers. Our aim was to develop a fast and accurate trio parentage assignment method for dense SNP data without prior genotyping error- or call rate knowledge among loci and individuals. This genomic relationship likelihood (GRL) method infers parentage by using genomic relationships, which are typically used in genomic prediction models. Results Using 50 simulated datasets with 53,427 to 55,517 SNPs, genotyping error rates of 1–3% and call rates of ~ 80 to 98%, GRL was found to be fast and highly (~ 99%) accurate for parentage assignment. An iterative approach was developed for training using the evaluation data, giving similar accuracy. For comparison, we used the Colony2 software that assigns parentage and sibship simultaneously to increase the power of the likelihood-based method and found that it has considerably lower accuracy than GRL. We also compared GRL with an exclusion-based method in which one of the parameters was estimated using GRL assignments.This method was slightly more accurate than GRL. Conclusions We show that GRL is a fast and accurate method of parentage assignment that can use dense, non-independent SNPs, with variable call rates and unknown genotyping error rates. By offering an alternative way of assigning parents, GRL is also suitable for estimating the expected proportion of inconsistent parent–offspring genotypes for exclusion-based models.http://link.springer.com/article/10.1186/s12711-018-0397-7
collection DOAJ
language deu
format Article
sources DOAJ
author Kim E. Grashei
Jørgen Ødegård
Theo H. E. Meuwissen
spellingShingle Kim E. Grashei
Jørgen Ødegård
Theo H. E. Meuwissen
Using genomic relationship likelihood for parentage assignment
Genetics Selection Evolution
author_facet Kim E. Grashei
Jørgen Ødegård
Theo H. E. Meuwissen
author_sort Kim E. Grashei
title Using genomic relationship likelihood for parentage assignment
title_short Using genomic relationship likelihood for parentage assignment
title_full Using genomic relationship likelihood for parentage assignment
title_fullStr Using genomic relationship likelihood for parentage assignment
title_full_unstemmed Using genomic relationship likelihood for parentage assignment
title_sort using genomic relationship likelihood for parentage assignment
publisher BMC
series Genetics Selection Evolution
issn 1297-9686
publishDate 2018-05-01
description Abstract Background Parentage assignment is usually based on a limited number of unlinked, independent genomic markers (microsatellites, low-density single nucleotide polymorphisms (SNPs), etc.). Classical methods for parentage assignment are exclusion-based (i.e. based on loci that violate Mendelian inheritance) or likelihood-based, assuming independent inheritance of loci. For true parent–offspring relations, genotyping errors cause apparent violations of Mendelian inheritance. Thus, the maximum proportion of such violations must be determined, which is complicated by variable call- and genotype error rates among loci and individuals. Recently, genotyping using high-density SNP chips has become available at lower cost and is increasingly used in genetics research and breeding programs. However, dense SNPs are not independently inherited, violating the assumptions of the likelihood-based methods. Hence, parentage assignment usually assumes a maximum proportion of exclusions, or applies likelihood-based methods on a smaller subset of independent markers. Our aim was to develop a fast and accurate trio parentage assignment method for dense SNP data without prior genotyping error- or call rate knowledge among loci and individuals. This genomic relationship likelihood (GRL) method infers parentage by using genomic relationships, which are typically used in genomic prediction models. Results Using 50 simulated datasets with 53,427 to 55,517 SNPs, genotyping error rates of 1–3% and call rates of ~ 80 to 98%, GRL was found to be fast and highly (~ 99%) accurate for parentage assignment. An iterative approach was developed for training using the evaluation data, giving similar accuracy. For comparison, we used the Colony2 software that assigns parentage and sibship simultaneously to increase the power of the likelihood-based method and found that it has considerably lower accuracy than GRL. We also compared GRL with an exclusion-based method in which one of the parameters was estimated using GRL assignments.This method was slightly more accurate than GRL. Conclusions We show that GRL is a fast and accurate method of parentage assignment that can use dense, non-independent SNPs, with variable call rates and unknown genotyping error rates. By offering an alternative way of assigning parents, GRL is also suitable for estimating the expected proportion of inconsistent parent–offspring genotypes for exclusion-based models.
url http://link.springer.com/article/10.1186/s12711-018-0397-7
work_keys_str_mv AT kimegrashei usinggenomicrelationshiplikelihoodforparentageassignment
AT jørgenødegard usinggenomicrelationshiplikelihoodforparentageassignment
AT theohemeuwissen usinggenomicrelationshiplikelihoodforparentageassignment
_version_ 1725279991534452736