Genomic variants revealed by invariably missing genotypes in nelore cattle.

Detalhes bibliográficos
Autor(a) principal: SILVA, J. M. da
Data de Publicação: 2015
Outros Autores: GIACHETTO, P. F., SILVA, L. O. C. da, CINTRA, L. C., PAIVA, S. R., CAETANO, A. R., YAMAGISHI, M. E. B.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
Texto Completo: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1033982
Resumo: High density genotyping panels have been used in a wide range of applications. From population genetics to genome-wide association studies, this technology still offers the lowest cost and the most consistent solution for generating SNP data. However, in spite of the application, part of the generated data is always discarded from final datasets based on quality control criteria used to remove unreliable markers. Some discarded data consists of markers that failed to generate genotypes, labeled as missing genotypes. A subset of missing genotypes that occur in the whole population under study may be caused by technical issues but can also be explained by the presence of genomic variations that are in the vicinity of the assayed SNP and that prevent genotyping probes from annealing. The latter case may contain relevant information because these missing genotypes might be used to identify population-specific genomic variants. In order to assess which case is more prevalent, we used Illumina HD Bovine chip genotypes from 1,709 Nelore (Bos indicus) samples. We found 3,200 missing genotypes among the whole population. NGS re-sequencing data from 8 sires were used to verify the presence of genomic variations within their flanking regions in 81.56% of these missing genotypes. Furthermore, we discovered 3,300 novel SNPs/Indels, 31% of which are located in genes that may affect traits of importance for the genetic improvement of cattle production.
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spelling Genomic variants revealed by invariably missing genotypes in nelore cattle.Polimorfismo de nucleotídeo únicoSequenciamento de DNAGado de corteBos IndicusSingle nucleotide polymorphismSequence analysisCattleHigh density genotyping panels have been used in a wide range of applications. From population genetics to genome-wide association studies, this technology still offers the lowest cost and the most consistent solution for generating SNP data. However, in spite of the application, part of the generated data is always discarded from final datasets based on quality control criteria used to remove unreliable markers. Some discarded data consists of markers that failed to generate genotypes, labeled as missing genotypes. A subset of missing genotypes that occur in the whole population under study may be caused by technical issues but can also be explained by the presence of genomic variations that are in the vicinity of the assayed SNP and that prevent genotyping probes from annealing. The latter case may contain relevant information because these missing genotypes might be used to identify population-specific genomic variants. In order to assess which case is more prevalent, we used Illumina HD Bovine chip genotypes from 1,709 Nelore (Bos indicus) samples. We found 3,200 missing genotypes among the whole population. NGS re-sequencing data from 8 sires were used to verify the presence of genomic variations within their flanking regions in 81.56% of these missing genotypes. Furthermore, we discovered 3,300 novel SNPs/Indels, 31% of which are located in genes that may affect traits of importance for the genetic improvement of cattle production.JOAQUIM MANOEL DA SILVA, Unemat; POLIANA FERNANDA GIACHETTO, CNPTIA; LUIZ OTÁVIO CAMPOS DA SILVA, CNPGC; LEANDRO CARRIJO CINTRA, CNPTIA; SAMUEL REZENDE PAIVA, SRI; ALEXANDRE RODRIGUES CAETANO, CENARGEN; MICHEL EDUARDO BELEZA YAMAGISHI, CNPTIA.SILVA, J. M. daGIACHETTO, P. F.SILVA, L. O. C. daCINTRA, L. C.PAIVA, S. R.CAETANO, A. R.YAMAGISHI, M. E. B.2016-01-15T11:11:11Z2016-01-15T11:11:11Z2016-01-1520152016-03-17T11:11:11Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlePlos One, San Francisco, v. 10, n. 8, p. 1-18, Aug. 2015.http://www.alice.cnptia.embrapa.br/alice/handle/doc/103398210.1371/journal.pone.0136035enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2017-08-16T03:31:10Zoai:www.alice.cnptia.embrapa.br:doc/1033982Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542017-08-16T03:31:10falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542017-08-16T03:31:10Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false
dc.title.none.fl_str_mv Genomic variants revealed by invariably missing genotypes in nelore cattle.
title Genomic variants revealed by invariably missing genotypes in nelore cattle.
spellingShingle Genomic variants revealed by invariably missing genotypes in nelore cattle.
SILVA, J. M. da
Polimorfismo de nucleotídeo único
Sequenciamento de DNA
Gado de corte
Bos Indicus
Single nucleotide polymorphism
Sequence analysis
Cattle
title_short Genomic variants revealed by invariably missing genotypes in nelore cattle.
title_full Genomic variants revealed by invariably missing genotypes in nelore cattle.
title_fullStr Genomic variants revealed by invariably missing genotypes in nelore cattle.
title_full_unstemmed Genomic variants revealed by invariably missing genotypes in nelore cattle.
title_sort Genomic variants revealed by invariably missing genotypes in nelore cattle.
author SILVA, J. M. da
author_facet SILVA, J. M. da
GIACHETTO, P. F.
SILVA, L. O. C. da
CINTRA, L. C.
PAIVA, S. R.
CAETANO, A. R.
YAMAGISHI, M. E. B.
author_role author
author2 GIACHETTO, P. F.
SILVA, L. O. C. da
CINTRA, L. C.
PAIVA, S. R.
CAETANO, A. R.
YAMAGISHI, M. E. B.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv JOAQUIM MANOEL DA SILVA, Unemat; POLIANA FERNANDA GIACHETTO, CNPTIA; LUIZ OTÁVIO CAMPOS DA SILVA, CNPGC; LEANDRO CARRIJO CINTRA, CNPTIA; SAMUEL REZENDE PAIVA, SRI; ALEXANDRE RODRIGUES CAETANO, CENARGEN; MICHEL EDUARDO BELEZA YAMAGISHI, CNPTIA.
dc.contributor.author.fl_str_mv SILVA, J. M. da
GIACHETTO, P. F.
SILVA, L. O. C. da
CINTRA, L. C.
PAIVA, S. R.
CAETANO, A. R.
YAMAGISHI, M. E. B.
dc.subject.por.fl_str_mv Polimorfismo de nucleotídeo único
Sequenciamento de DNA
Gado de corte
Bos Indicus
Single nucleotide polymorphism
Sequence analysis
Cattle
topic Polimorfismo de nucleotídeo único
Sequenciamento de DNA
Gado de corte
Bos Indicus
Single nucleotide polymorphism
Sequence analysis
Cattle
description High density genotyping panels have been used in a wide range of applications. From population genetics to genome-wide association studies, this technology still offers the lowest cost and the most consistent solution for generating SNP data. However, in spite of the application, part of the generated data is always discarded from final datasets based on quality control criteria used to remove unreliable markers. Some discarded data consists of markers that failed to generate genotypes, labeled as missing genotypes. A subset of missing genotypes that occur in the whole population under study may be caused by technical issues but can also be explained by the presence of genomic variations that are in the vicinity of the assayed SNP and that prevent genotyping probes from annealing. The latter case may contain relevant information because these missing genotypes might be used to identify population-specific genomic variants. In order to assess which case is more prevalent, we used Illumina HD Bovine chip genotypes from 1,709 Nelore (Bos indicus) samples. We found 3,200 missing genotypes among the whole population. NGS re-sequencing data from 8 sires were used to verify the presence of genomic variations within their flanking regions in 81.56% of these missing genotypes. Furthermore, we discovered 3,300 novel SNPs/Indels, 31% of which are located in genes that may affect traits of importance for the genetic improvement of cattle production.
publishDate 2015
dc.date.none.fl_str_mv 2015
2016-01-15T11:11:11Z
2016-01-15T11:11:11Z
2016-01-15
2016-03-17T11:11:11Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Plos One, San Francisco, v. 10, n. 8, p. 1-18, Aug. 2015.
http://www.alice.cnptia.embrapa.br/alice/handle/doc/1033982
10.1371/journal.pone.0136035
identifier_str_mv Plos One, San Francisco, v. 10, n. 8, p. 1-18, Aug. 2015.
10.1371/journal.pone.0136035
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/1033982
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
instacron:EMBRAPA
instname_str Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
instacron_str EMBRAPA
institution EMBRAPA
reponame_str Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
collection Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
repository.name.fl_str_mv Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
repository.mail.fl_str_mv cg-riaa@embrapa.br
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