Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing

Detalhes bibliográficos
Autor(a) principal: Valle-Silva, Guilherme do
Data de Publicação: 2019
Outros Autores: Souza, Flávia Djenane Nunes de, Marcorin, Letícia, Pereira, Alison Luis Eburneo, Carratto, Thássia Mayra Telles, Debortoli, Guilherme, Oliveira, Maria Luiza Guimarães de, Fracasso, Nádia Carolina de Aguiar, Andrade, Edilene Santos de, Donadi, Eduardo Antônio, Norton, Heather L., Parra, Esteban J., Simões, Aguinaldo Luiz, Castelli, Erick C. [UNESP], Mendes-Junior, Celso Teixeira
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.fsigen.2019.03.003
http://hdl.handle.net/11449/189698
Resumo: SNP analysis is of paramount importance in forensic genetics. The development of new technologies in next-generation sequencing allowed processing a large number of markers in various samples simultaneously. Although SNPs are less informative than STRs, they present lower mutation rates and perform better when using degraded samples. Some SNP systems were developed for forensic usage, such as the SNPforID 52-plex, from the SNPforID Consortium, containing 52 bi-allelic SNPs for human identification. In this paper we evaluated the informativeness of this system in a Brazilian population sample (n = 340). DNA libraries were prepared using a customized HaloPlex Target Enrichment System kit (Agilent Technologies, Inc.) and sequenced in the MiSeq Personal Sequencer platform (Illumina Inc.). The methodology presented here allowed the analysis of 51 out of 52 SNPforID markers. Allele frequencies and forensic parameters were estimated, revealing high informativeness: the combined match probability and power of exclusion were 6.48 × 10 −21 and 0.9997, respectively. Population admixture analysis indicates high European contribution (more than 70%) and low Amerindian contribution (less than 10%) in our population, while individual admixture analyses were consistent with the majority of individuals presenting high European contribution. This study demonstrates that the 52-plex kit is suitable for forensic cases in a Brazilian population, presenting results comparable with those obtained using a 16 STR panel.
id UNSP_ca0df0596b1ed76ce853c2e3ecbdec46
oai_identifier_str oai:repositorio.unesp.br:11449/189698
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencingBrazilForensic geneticsGenetic admixtureMassively-parallel sequencingSNPforID 52-plexSNPsSNP analysis is of paramount importance in forensic genetics. The development of new technologies in next-generation sequencing allowed processing a large number of markers in various samples simultaneously. Although SNPs are less informative than STRs, they present lower mutation rates and perform better when using degraded samples. Some SNP systems were developed for forensic usage, such as the SNPforID 52-plex, from the SNPforID Consortium, containing 52 bi-allelic SNPs for human identification. In this paper we evaluated the informativeness of this system in a Brazilian population sample (n = 340). DNA libraries were prepared using a customized HaloPlex Target Enrichment System kit (Agilent Technologies, Inc.) and sequenced in the MiSeq Personal Sequencer platform (Illumina Inc.). The methodology presented here allowed the analysis of 51 out of 52 SNPforID markers. Allele frequencies and forensic parameters were estimated, revealing high informativeness: the combined match probability and power of exclusion were 6.48 × 10 −21 and 0.9997, respectively. Population admixture analysis indicates high European contribution (more than 70%) and low Amerindian contribution (less than 10%) in our population, while individual admixture analyses were consistent with the majority of individuals presenting high European contribution. This study demonstrates that the 52-plex kit is suitable for forensic cases in a Brazilian population, presenting results comparable with those obtained using a 16 STR panel.National Institute of JusticeFundação de Amparo à Pesquisa do Estado de GoiásCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Natural Sciences and Engineering Research Council of CanadaDepartamento de Química Laboratório de Pesquisas Forenses e Genômicas Faculdade de Filosofia Ciências e Letras de Ribeirão Preto Universidade de São PauloDepartamento de Genética Faculdade de Medicina de Ribeirão Preto Universidade de São PauloDepartment of Anthropology University of Toronto at MississaugaMolecular Oncology Research Center Barretos Cancer HospitalDivisão de Imunologia Clínica Departamento de Clínica Médica Faculdade de Medicina de Ribeirão Preto Universidade de São PauloDepartment of Anthropology University of CincinnatiSão Paulo State University (UNESP) Department of Pathology School of MedicineSão Paulo State University (UNESP) Department of Pathology School of MedicineNational Institute of Justice: # 2013-DN-BX-K011Fundação de Amparo à Pesquisa do Estado de Goiás: #2013/15447-0CAPES: #302590/2016-1CNPq: #448242/2014-1CAPES: (#304931/2014-1CAPES: (#309572/2014-2Universidade de São Paulo (USP)University of Toronto at MississaugaBarretos Cancer HospitalUniversity of CincinnatiUniversidade Estadual Paulista (Unesp)Valle-Silva, Guilherme doSouza, Flávia Djenane Nunes deMarcorin, LetíciaPereira, Alison Luis EburneoCarratto, Thássia Mayra TellesDebortoli, GuilhermeOliveira, Maria Luiza Guimarães deFracasso, Nádia Carolina de AguiarAndrade, Edilene Santos deDonadi, Eduardo AntônioNorton, Heather L.Parra, Esteban J.Simões, Aguinaldo LuizCastelli, Erick C. [UNESP]Mendes-Junior, Celso Teixeira2019-10-06T16:49:19Z2019-10-06T16:49:19Z2019-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article201-209http://dx.doi.org/10.1016/j.fsigen.2019.03.003Forensic Science International: Genetics, v. 40, p. 201-209.1878-03261872-4973http://hdl.handle.net/11449/18969810.1016/j.fsigen.2019.03.0032-s2.0-85062916063Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengForensic Science International: Geneticsinfo:eu-repo/semantics/openAccess2021-10-22T19:11:01Zoai:repositorio.unesp.br:11449/189698Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:38:58.638328Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
title Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
spellingShingle Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
Valle-Silva, Guilherme do
Brazil
Forensic genetics
Genetic admixture
Massively-parallel sequencing
SNPforID 52-plex
SNPs
title_short Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
title_full Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
title_fullStr Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
title_full_unstemmed Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
title_sort Applicability of the SNPforID 52-plex panel for human identification and ancestry evaluation in a Brazilian population sample by next-generation sequencing
author Valle-Silva, Guilherme do
author_facet Valle-Silva, Guilherme do
Souza, Flávia Djenane Nunes de
Marcorin, Letícia
Pereira, Alison Luis Eburneo
Carratto, Thássia Mayra Telles
Debortoli, Guilherme
Oliveira, Maria Luiza Guimarães de
Fracasso, Nádia Carolina de Aguiar
Andrade, Edilene Santos de
Donadi, Eduardo Antônio
Norton, Heather L.
Parra, Esteban J.
Simões, Aguinaldo Luiz
Castelli, Erick C. [UNESP]
Mendes-Junior, Celso Teixeira
author_role author
author2 Souza, Flávia Djenane Nunes de
Marcorin, Letícia
Pereira, Alison Luis Eburneo
Carratto, Thássia Mayra Telles
Debortoli, Guilherme
Oliveira, Maria Luiza Guimarães de
Fracasso, Nádia Carolina de Aguiar
Andrade, Edilene Santos de
Donadi, Eduardo Antônio
Norton, Heather L.
Parra, Esteban J.
Simões, Aguinaldo Luiz
Castelli, Erick C. [UNESP]
Mendes-Junior, Celso Teixeira
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
University of Toronto at Mississauga
Barretos Cancer Hospital
University of Cincinnati
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Valle-Silva, Guilherme do
Souza, Flávia Djenane Nunes de
Marcorin, Letícia
Pereira, Alison Luis Eburneo
Carratto, Thássia Mayra Telles
Debortoli, Guilherme
Oliveira, Maria Luiza Guimarães de
Fracasso, Nádia Carolina de Aguiar
Andrade, Edilene Santos de
Donadi, Eduardo Antônio
Norton, Heather L.
Parra, Esteban J.
Simões, Aguinaldo Luiz
Castelli, Erick C. [UNESP]
Mendes-Junior, Celso Teixeira
dc.subject.por.fl_str_mv Brazil
Forensic genetics
Genetic admixture
Massively-parallel sequencing
SNPforID 52-plex
SNPs
topic Brazil
Forensic genetics
Genetic admixture
Massively-parallel sequencing
SNPforID 52-plex
SNPs
description SNP analysis is of paramount importance in forensic genetics. The development of new technologies in next-generation sequencing allowed processing a large number of markers in various samples simultaneously. Although SNPs are less informative than STRs, they present lower mutation rates and perform better when using degraded samples. Some SNP systems were developed for forensic usage, such as the SNPforID 52-plex, from the SNPforID Consortium, containing 52 bi-allelic SNPs for human identification. In this paper we evaluated the informativeness of this system in a Brazilian population sample (n = 340). DNA libraries were prepared using a customized HaloPlex Target Enrichment System kit (Agilent Technologies, Inc.) and sequenced in the MiSeq Personal Sequencer platform (Illumina Inc.). The methodology presented here allowed the analysis of 51 out of 52 SNPforID markers. Allele frequencies and forensic parameters were estimated, revealing high informativeness: the combined match probability and power of exclusion were 6.48 × 10 −21 and 0.9997, respectively. Population admixture analysis indicates high European contribution (more than 70%) and low Amerindian contribution (less than 10%) in our population, while individual admixture analyses were consistent with the majority of individuals presenting high European contribution. This study demonstrates that the 52-plex kit is suitable for forensic cases in a Brazilian population, presenting results comparable with those obtained using a 16 STR panel.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-06T16:49:19Z
2019-10-06T16:49:19Z
2019-05-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.fsigen.2019.03.003
Forensic Science International: Genetics, v. 40, p. 201-209.
1878-0326
1872-4973
http://hdl.handle.net/11449/189698
10.1016/j.fsigen.2019.03.003
2-s2.0-85062916063
url http://dx.doi.org/10.1016/j.fsigen.2019.03.003
http://hdl.handle.net/11449/189698
identifier_str_mv Forensic Science International: Genetics, v. 40, p. 201-209.
1878-0326
1872-4973
10.1016/j.fsigen.2019.03.003
2-s2.0-85062916063
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Forensic Science International: Genetics
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 201-209
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808129343827738624