Cargando…

Imputation for sequencing variants preselected to a customized low-density chip

The sequencing variants preselected from association analyses and bioinformatics analyses could improve genomic prediction. In this study, the imputation of sequencing SNPs preselected from major dairy breeds in Denmark-Finland-Sweden (DFS) and France (FRA) was investigated for both contemporary ani...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Aoxing, Lund, Mogens Sandø, Boichard, Didier, Mao, Xiaowei, Karaman, Emre, Fritz, Sebastien, Aamand, Gert Pedersen, Wang, Yachun, Su, Guosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293337/
https://www.ncbi.nlm.nih.gov/pubmed/32533087
http://dx.doi.org/10.1038/s41598-020-66523-7
_version_ 1783546282539745280
author Liu, Aoxing
Lund, Mogens Sandø
Boichard, Didier
Mao, Xiaowei
Karaman, Emre
Fritz, Sebastien
Aamand, Gert Pedersen
Wang, Yachun
Su, Guosheng
author_facet Liu, Aoxing
Lund, Mogens Sandø
Boichard, Didier
Mao, Xiaowei
Karaman, Emre
Fritz, Sebastien
Aamand, Gert Pedersen
Wang, Yachun
Su, Guosheng
author_sort Liu, Aoxing
collection PubMed
description The sequencing variants preselected from association analyses and bioinformatics analyses could improve genomic prediction. In this study, the imputation of sequencing SNPs preselected from major dairy breeds in Denmark-Finland-Sweden (DFS) and France (FRA) was investigated for both contemporary animals and old bulls in Danish Jersey. For contemporary animals, a two-step imputation which first imputed to 54 K and then to 54 K + DFS + FRA SNPs achieved highest accuracy. Correlations between observed and imputed genotypes were 91.6% for DFS SNPs and 87.6% for FRA SNPs, while concordance rates were 96.6% for DFS SNPs and 93.5% for FRA SNPs. The SNPs with lower minor allele frequency (MAF) tended to have lower correlations but higher concordance rates. For old bulls, imputation for DFS and FRA SNPs were relatively accurate even for bulls without progenies (correlations higher than 97.2% and concordance rates higher than 98.4%). For contemporary animals, given limited imputation accuracy of preselected sequencing SNPs especially for SNPs with low MAF, it would be a good strategy to directly genotype preselected sequencing SNPs with a customized SNP chip. For old bulls, given high imputation accuracy for preselected sequencing SNPs with all MAF ranges, it would be unnecessary to re-genotype preselected sequencing SNPs.
format Online
Article
Text
id pubmed-7293337
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-72933372020-06-17 Imputation for sequencing variants preselected to a customized low-density chip Liu, Aoxing Lund, Mogens Sandø Boichard, Didier Mao, Xiaowei Karaman, Emre Fritz, Sebastien Aamand, Gert Pedersen Wang, Yachun Su, Guosheng Sci Rep Article The sequencing variants preselected from association analyses and bioinformatics analyses could improve genomic prediction. In this study, the imputation of sequencing SNPs preselected from major dairy breeds in Denmark-Finland-Sweden (DFS) and France (FRA) was investigated for both contemporary animals and old bulls in Danish Jersey. For contemporary animals, a two-step imputation which first imputed to 54 K and then to 54 K + DFS + FRA SNPs achieved highest accuracy. Correlations between observed and imputed genotypes were 91.6% for DFS SNPs and 87.6% for FRA SNPs, while concordance rates were 96.6% for DFS SNPs and 93.5% for FRA SNPs. The SNPs with lower minor allele frequency (MAF) tended to have lower correlations but higher concordance rates. For old bulls, imputation for DFS and FRA SNPs were relatively accurate even for bulls without progenies (correlations higher than 97.2% and concordance rates higher than 98.4%). For contemporary animals, given limited imputation accuracy of preselected sequencing SNPs especially for SNPs with low MAF, it would be a good strategy to directly genotype preselected sequencing SNPs with a customized SNP chip. For old bulls, given high imputation accuracy for preselected sequencing SNPs with all MAF ranges, it would be unnecessary to re-genotype preselected sequencing SNPs. Nature Publishing Group UK 2020-06-12 /pmc/articles/PMC7293337/ /pubmed/32533087 http://dx.doi.org/10.1038/s41598-020-66523-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liu, Aoxing
Lund, Mogens Sandø
Boichard, Didier
Mao, Xiaowei
Karaman, Emre
Fritz, Sebastien
Aamand, Gert Pedersen
Wang, Yachun
Su, Guosheng
Imputation for sequencing variants preselected to a customized low-density chip
title Imputation for sequencing variants preselected to a customized low-density chip
title_full Imputation for sequencing variants preselected to a customized low-density chip
title_fullStr Imputation for sequencing variants preselected to a customized low-density chip
title_full_unstemmed Imputation for sequencing variants preselected to a customized low-density chip
title_short Imputation for sequencing variants preselected to a customized low-density chip
title_sort imputation for sequencing variants preselected to a customized low-density chip
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293337/
https://www.ncbi.nlm.nih.gov/pubmed/32533087
http://dx.doi.org/10.1038/s41598-020-66523-7
work_keys_str_mv AT liuaoxing imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT lundmogenssandø imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT boicharddidier imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT maoxiaowei imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT karamanemre imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT fritzsebastien imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT aamandgertpedersen imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT wangyachun imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip
AT suguosheng imputationforsequencingvariantspreselectedtoacustomizedlowdensitychip