Applications of massively parallel sequencing in forensic genetics

Detalhes bibliográficos
Autor(a) principal: Carratto,Thássia Mayra Telles
Data de Publicação: 2022
Outros Autores: Moraes,Vitor Matheus Soares, Recalde,Tamara Soledad Frontanilla, Oliveira,Maria Luiza Guimarães de, Teixeira Mendes-Junior,Celso
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Genetics and Molecular Biology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572022000400105
Resumo: Abstract Massively parallel sequencing, also referred to as next-generation sequencing, has positively changed DNA analysis, allowing further advances in genetics. Its capability of dealing with low quantity/damaged samples makes it an interesting instrument for forensics. The main advantage of MPS is the possibility of analyzing simultaneously thousands of genetic markers, generating high-resolution data. Its detailed sequence information allowed the discovery of variations in core forensic short tandem repeat loci, as well as the identification of previous unknown polymorphisms. Furthermore, different types of markers can be sequenced in a single run, enabling the emergence of DIP-STRs, SNP-STR haplotypes, and microhaplotypes, which can be very useful in mixture deconvolution cases. In addition, the multiplex analysis of different single nucleotide polymorphisms can provide valuable information about identity, biogeographic ancestry, paternity, or phenotype. DNA methylation patterns, mitochondrial DNA, mRNA, and microRNA profiling can also be analyzed for different purposes, such as age inference, maternal lineage analysis, body-fluid identification, and monozygotic twin discrimination. MPS technology also empowers the study of metagenomics, which analyzes genetic material from a microbial community to obtain information about individual identification, post-mortem interval estimation, geolocation inference, and substrate analysis. This review aims to discuss the main applications of MPS in forensic genetics.
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spelling Applications of massively parallel sequencing in forensic geneticsNext-Generation Sequencing (NGS)DNA analysisRNA analysismethylationgenetic polymorphismsAbstract Massively parallel sequencing, also referred to as next-generation sequencing, has positively changed DNA analysis, allowing further advances in genetics. Its capability of dealing with low quantity/damaged samples makes it an interesting instrument for forensics. The main advantage of MPS is the possibility of analyzing simultaneously thousands of genetic markers, generating high-resolution data. Its detailed sequence information allowed the discovery of variations in core forensic short tandem repeat loci, as well as the identification of previous unknown polymorphisms. Furthermore, different types of markers can be sequenced in a single run, enabling the emergence of DIP-STRs, SNP-STR haplotypes, and microhaplotypes, which can be very useful in mixture deconvolution cases. In addition, the multiplex analysis of different single nucleotide polymorphisms can provide valuable information about identity, biogeographic ancestry, paternity, or phenotype. DNA methylation patterns, mitochondrial DNA, mRNA, and microRNA profiling can also be analyzed for different purposes, such as age inference, maternal lineage analysis, body-fluid identification, and monozygotic twin discrimination. MPS technology also empowers the study of metagenomics, which analyzes genetic material from a microbial community to obtain information about individual identification, post-mortem interval estimation, geolocation inference, and substrate analysis. This review aims to discuss the main applications of MPS in forensic genetics.Sociedade Brasileira de Genética2022-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572022000400105Genetics and Molecular Biology v.45 n.3 suppl.1 2022reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/1678-4685-gmb-2022-0077info:eu-repo/semantics/openAccessCarratto,Thássia Mayra TellesMoraes,Vitor Matheus SoaresRecalde,Tamara Soledad FrontanillaOliveira,Maria Luiza Guimarães deTeixeira Mendes-Junior,Celsoeng2022-09-15T00:00:00Zoai:scielo:S1415-47572022000400105Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2022-09-15T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false
dc.title.none.fl_str_mv Applications of massively parallel sequencing in forensic genetics
title Applications of massively parallel sequencing in forensic genetics
spellingShingle Applications of massively parallel sequencing in forensic genetics
Carratto,Thássia Mayra Telles
Next-Generation Sequencing (NGS)
DNA analysis
RNA analysis
methylation
genetic polymorphisms
title_short Applications of massively parallel sequencing in forensic genetics
title_full Applications of massively parallel sequencing in forensic genetics
title_fullStr Applications of massively parallel sequencing in forensic genetics
title_full_unstemmed Applications of massively parallel sequencing in forensic genetics
title_sort Applications of massively parallel sequencing in forensic genetics
author Carratto,Thássia Mayra Telles
author_facet Carratto,Thássia Mayra Telles
Moraes,Vitor Matheus Soares
Recalde,Tamara Soledad Frontanilla
Oliveira,Maria Luiza Guimarães de
Teixeira Mendes-Junior,Celso
author_role author
author2 Moraes,Vitor Matheus Soares
Recalde,Tamara Soledad Frontanilla
Oliveira,Maria Luiza Guimarães de
Teixeira Mendes-Junior,Celso
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Carratto,Thássia Mayra Telles
Moraes,Vitor Matheus Soares
Recalde,Tamara Soledad Frontanilla
Oliveira,Maria Luiza Guimarães de
Teixeira Mendes-Junior,Celso
dc.subject.por.fl_str_mv Next-Generation Sequencing (NGS)
DNA analysis
RNA analysis
methylation
genetic polymorphisms
topic Next-Generation Sequencing (NGS)
DNA analysis
RNA analysis
methylation
genetic polymorphisms
description Abstract Massively parallel sequencing, also referred to as next-generation sequencing, has positively changed DNA analysis, allowing further advances in genetics. Its capability of dealing with low quantity/damaged samples makes it an interesting instrument for forensics. The main advantage of MPS is the possibility of analyzing simultaneously thousands of genetic markers, generating high-resolution data. Its detailed sequence information allowed the discovery of variations in core forensic short tandem repeat loci, as well as the identification of previous unknown polymorphisms. Furthermore, different types of markers can be sequenced in a single run, enabling the emergence of DIP-STRs, SNP-STR haplotypes, and microhaplotypes, which can be very useful in mixture deconvolution cases. In addition, the multiplex analysis of different single nucleotide polymorphisms can provide valuable information about identity, biogeographic ancestry, paternity, or phenotype. DNA methylation patterns, mitochondrial DNA, mRNA, and microRNA profiling can also be analyzed for different purposes, such as age inference, maternal lineage analysis, body-fluid identification, and monozygotic twin discrimination. MPS technology also empowers the study of metagenomics, which analyzes genetic material from a microbial community to obtain information about individual identification, post-mortem interval estimation, geolocation inference, and substrate analysis. This review aims to discuss the main applications of MPS in forensic genetics.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572022000400105
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572022000400105
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-4685-gmb-2022-0077
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Genética
publisher.none.fl_str_mv Sociedade Brasileira de Genética
dc.source.none.fl_str_mv Genetics and Molecular Biology v.45 n.3 suppl.1 2022
reponame:Genetics and Molecular Biology
instname:Sociedade Brasileira de Genética (SBG)
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instname_str Sociedade Brasileira de Genética (SBG)
instacron_str SBG
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reponame_str Genetics and Molecular Biology
collection Genetics and Molecular Biology
repository.name.fl_str_mv Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)
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