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dc.contributor.author
Ballantyne, Kaye N.
dc.contributor.author
Ralf, Arwin
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Aboukhalid, Rachid
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Achakzai, Niaz M.
dc.contributor.author
Anjos, Maria J.
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Bobillo, Maria Cecilia
dc.contributor.author
Daniel Corach
dc.contributor.author
Sala, Adriana Andrea
dc.contributor.author
Sirker, Miriam
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Siváková, Daniela
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Škaro, Vedrana
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Solano Matamoros, Carlos
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Souto, Luis
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Stenzl, Vlastimil
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Sudoyo, Herawati
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Syndercombe Court, Denise
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Tagliabracci, Adriano
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Taylor, Duncan
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Tillmar, Andreas
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Tsybovsky, Iosif S.
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Tyler Smith, Chris
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Gaag, Kristiaan J. van der
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Vanek, Daniel
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Völgyi, Antónia
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Ward, Denise
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Willemse, Patricia
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Yap, Eric P. H.
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Yong, Rita Y. Y.
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Zupanič Pajnič, Irena
dc.contributor.author
Kayser, Manfred
dc.date.available
2017-12-12T20:40:22Z
dc.date.issued
2014-07
dc.identifier.citation
Ballantyne, Kaye N.; Ralf, Arwin; Aboukhalid, Rachid; Achakzai, Niaz M.; Anjos, Maria J.; et al.; Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats; Wiley; Human Mutation; 35; 8; 7-2014; 1021-1032
dc.identifier.issn
1059-7794
dc.identifier.uri
http://hdl.handle.net/11336/30345
dc.description.abstract
Relevant for various areas of human genetics, Y-chromosomal short tandem repeats (Y-STRs) are commonly used for testing close paternal relationships among individuals and populations, and for male lineage identification. However, even the widely used 17-loci Yfiler set cannot resolve individuals and populations completely. Here, 52 centers generated quality-controlled data of 13 rapidly mutating (RM) Y-STRs in 14,644 related and unrelated males from 111 worldwide populations. Strikingly, >99% of the 12,272 unrelated males were completely individualized. Haplotype diversity was extremely high (global: 0.9999985, regional: 0.99836–0.9999988). Haplotype sharing between populations was almost absent except for six (0.05%) of the 12,156 haplotypes. Haplotype sharing within populations was generally rare (0.8% nonunique haplotypes), significantly lower in urban (0.9%) than rural (2.1%) and highest in endogamous groups (14.3%). Analysis of molecular variance revealed 99.98% of variation within populations, 0.018% among populations within groups, and 0.002% among groups. Of the 2,372 newly and 156 previously typed male relative pairs, 29% were differentiated including 27% of the 2,378 father–son pairs. Relative to Yfiler, haplotype diversity was increased in 86% of the populations tested and overall male relative differentiation was raised by 23.5%. Our study demonstrates the value of RM Y-STRs in identifying and separating unrelated and related males and provides a reference database.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Wiley
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/
dc.subject
Y-Str
dc.subject
Rapid Mutation
dc.subject.classification
Medicina Forense
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Otras Ciencias Médicas
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CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2017-12-12T18:28:17Z
dc.journal.volume
35
dc.journal.number
8
dc.journal.pagination
1021-1032
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Nueva York
dc.description.fil
Fil: Ballantyne, Kaye N.. Erasmus MC University Medical Centre Rotterdam; Países Bajos
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Fil: Ralf, Arwin. Erasmus MC University Medical Centre Rotterdam; Países Bajos
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Fil: Aboukhalid, Rachid. Mohammed V Agdal University; Marruecos
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Fil: Achakzai, Niaz M.. University of the Punjab; Pakistán
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Fil: Anjos, Maria J.. National Institute of Legal Medicine and Forensic Sciences; Portugal
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Fil: Bobillo, Maria Cecilia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Servicio de Huellas Digitales Genéticas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
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Fil: Daniel Corach. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Servicio de Huellas Digitales Genéticas; Argentina
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Fil: Sala, Adriana Andrea. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Servicio de Huellas Digitales Genéticas; Argentina
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Fil: Sirker, Miriam. University of Cologne. Faculty of Medicine. Institute of Legal Medicine; Alemania
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Fil: Siváková, Daniela. University in Bratislava; Eslovaquia
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Fil: Škaro, Vedrana. Genos Ltd, Zagreb. DNA Laboratory; Croacia
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Fil: Solano Matamoros, Carlos. Universidad de Costa Rica; Costa Rica
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Fil: Souto, Luis. Universidade de Aveiro; Portugal
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Fil: Stenzl, Vlastimil. Institute of Criminalistics Prague; República Checa
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Fil: Sudoyo, Herawati. Eijkman Institute for Molecular Biology; Indonesia
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Fil: Syndercombe Court, Denise. King; Reino Unido
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Fil: Tagliabracci, Adriano. Università Politecnica delle Marche; Italia
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Fil: Taylor, Duncan. Flinders University; Australia
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Fil: Tillmar, Andreas. Linköping University; Suecia
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Fil: Tsybovsky, Iosif S.. Scientific and Practical Centre of the State Committee of Forensic Expertises; Bielorrusia
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Fil: Tyler Smith, Chris. The Wellcome Trust Sanger Institute. Wellcome Trust Genome Campus, ; Reino Unido
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Fil: Gaag, Kristiaan J. van der. Leiden University Medical Center. Department of Human Genetics; Países Bajos
dc.description.fil
Fil: Vanek, Daniel. Charles University. Institute of the Legal Medicine; República Checa. Forensic DNA Service; República Checa
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Fil: Völgyi, Antónia. Ministry of Public Administration and Justice; Hungría. Network of Forensic Science Institutes. Institute of Forensic Medicine. DNA Laboratory; Hungría
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Fil: Ward, Denise. Forensic Science South Australia; Australia
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Fil: Willemse, Patricia. Leiden University Medical Center; Países Bajos
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Fil: Yap, Eric P. H.. DSO National Laboratories. Defence Medical and Environmental Research Institute; Singapur
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Fil: Yong, Rita Y. Y.. DSO National Laboratories. Defence Medical and Environmental Research Institute; Singapur
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Fil: Zupanič Pajnič, Irena. University of Ljubljana. Faculty of Medicine. Institute of Forensic Medicine; Eslovenia
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Fil: Kayser, Manfred. Erasmus MC University Medical Centre Rotterdam; Países Bajos
dc.journal.title
Human Mutation
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/humu.22599
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145662/
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/humu.22599/abstract
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