New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.13/2980 |
Resumo: | A great amount of population and forensic genetic data are available for X-STRs supporting the need for having a common and accurate nomenclature among laboratories allowing for better communication, data exchange, and data comparison. DXS10148, DXS10074 and DXS10134 are commonly used X-STRs particularly due to their inclusion in the commercial kit Investigator Argus X-12 (Qiagen). Samples from West Africa and Iraq were sequenced for all three X-STRs allowing the detection of new DNA sequence variants. At DXS10148, variation was detected at four bases downstream from the flanking region from the repeat motif. The sequence AAGG-AAAG has been detected for the first time as a varying (AAGGAAAG)1–3 motif, in the present work. One additional string when compared to the common one (AAGGAAAG)2 adds eight bases to the fragment size of the tetranucleotide STR. This means that 2 repeats are added in these cases to the fragment size of the allele, while the presence of only one copy will reduce the expected allele size by 2 repeats. At DXS10074 two varying stretches consisting of AC and AG dinucleotide repeats were observed in the upstream flanking region, six bases from the main repeat core that also influence the expected allele size. DXS10134 revealed a simpler nomenclature in the Guinea-Bissau sample set when compared to the previously described allele nomenclature. This detected new hidden variation also has impact on the actual allele nomenclature at this locus as it contributes to a new class of short alleles so far undetected in other studies. |
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New sequence variants detected at DXS10148, DXS10074 and DXS10134 lociInvestigator Argus X-12X-STRsX chromosomeWest AfricaIraqGuinea-Bissau.Faculdade de Ciências da VidaA great amount of population and forensic genetic data are available for X-STRs supporting the need for having a common and accurate nomenclature among laboratories allowing for better communication, data exchange, and data comparison. DXS10148, DXS10074 and DXS10134 are commonly used X-STRs particularly due to their inclusion in the commercial kit Investigator Argus X-12 (Qiagen). Samples from West Africa and Iraq were sequenced for all three X-STRs allowing the detection of new DNA sequence variants. At DXS10148, variation was detected at four bases downstream from the flanking region from the repeat motif. The sequence AAGG-AAAG has been detected for the first time as a varying (AAGGAAAG)1–3 motif, in the present work. One additional string when compared to the common one (AAGGAAAG)2 adds eight bases to the fragment size of the tetranucleotide STR. This means that 2 repeats are added in these cases to the fragment size of the allele, while the presence of only one copy will reduce the expected allele size by 2 repeats. At DXS10074 two varying stretches consisting of AC and AG dinucleotide repeats were observed in the upstream flanking region, six bases from the main repeat core that also influence the expected allele size. DXS10134 revealed a simpler nomenclature in the Guinea-Bissau sample set when compared to the previously described allele nomenclature. This detected new hidden variation also has impact on the actual allele nomenclature at this locus as it contributes to a new class of short alleles so far undetected in other studies.International Society for Forensic Genetics (ISFG)DigitUMaGomes, IvaBrehm, AntónioGusmão, LeonorSchneider, Peter M.2020-11-13T15:47:09Z20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.13/2980engGomes, I., Brehm, A., Gusmão, L., & Schneider, P. M. (2016). New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci. Forensic Science International: Genetics, 20, 112-116.10.1016/j.fsigen.2015.10.005info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-26T03:38:20Zoai:digituma.uma.pt:10400.13/2980Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:05:49.257490Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci |
title |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci |
spellingShingle |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci Gomes, Iva Investigator Argus X-12 X-STRs X chromosome West Africa Iraq Guinea-Bissau . Faculdade de Ciências da Vida |
title_short |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci |
title_full |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci |
title_fullStr |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci |
title_full_unstemmed |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci |
title_sort |
New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci |
author |
Gomes, Iva |
author_facet |
Gomes, Iva Brehm, António Gusmão, Leonor Schneider, Peter M. |
author_role |
author |
author2 |
Brehm, António Gusmão, Leonor Schneider, Peter M. |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
DigitUMa |
dc.contributor.author.fl_str_mv |
Gomes, Iva Brehm, António Gusmão, Leonor Schneider, Peter M. |
dc.subject.por.fl_str_mv |
Investigator Argus X-12 X-STRs X chromosome West Africa Iraq Guinea-Bissau . Faculdade de Ciências da Vida |
topic |
Investigator Argus X-12 X-STRs X chromosome West Africa Iraq Guinea-Bissau . Faculdade de Ciências da Vida |
description |
A great amount of population and forensic genetic data are available for X-STRs supporting the need for having a common and accurate nomenclature among laboratories allowing for better communication, data exchange, and data comparison. DXS10148, DXS10074 and DXS10134 are commonly used X-STRs particularly due to their inclusion in the commercial kit Investigator Argus X-12 (Qiagen). Samples from West Africa and Iraq were sequenced for all three X-STRs allowing the detection of new DNA sequence variants. At DXS10148, variation was detected at four bases downstream from the flanking region from the repeat motif. The sequence AAGG-AAAG has been detected for the first time as a varying (AAGGAAAG)1–3 motif, in the present work. One additional string when compared to the common one (AAGGAAAG)2 adds eight bases to the fragment size of the tetranucleotide STR. This means that 2 repeats are added in these cases to the fragment size of the allele, while the presence of only one copy will reduce the expected allele size by 2 repeats. At DXS10074 two varying stretches consisting of AC and AG dinucleotide repeats were observed in the upstream flanking region, six bases from the main repeat core that also influence the expected allele size. DXS10134 revealed a simpler nomenclature in the Guinea-Bissau sample set when compared to the previously described allele nomenclature. This detected new hidden variation also has impact on the actual allele nomenclature at this locus as it contributes to a new class of short alleles so far undetected in other studies. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2016-01-01T00:00:00Z 2020-11-13T15:47:09Z |
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://hdl.handle.net/10400.13/2980 |
url |
http://hdl.handle.net/10400.13/2980 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Gomes, I., Brehm, A., Gusmão, L., & Schneider, P. M. (2016). New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci. Forensic Science International: Genetics, 20, 112-116. 10.1016/j.fsigen.2015.10.005 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
International Society for Forensic Genetics (ISFG) |
publisher.none.fl_str_mv |
International Society for Forensic Genetics (ISFG) |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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