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dc.contributor.authorZgonjanin-Bosić, Draganaen_US
dc.contributor.authorAlghafri, Rasheden_US
dc.contributor.authorAlmheiri, Reemen_US
dc.contributor.authorAntov, Mirjanaen_US
dc.contributor.authorToljić, Dankaen_US
dc.contributor.authorVuković, Radenkoen_US
dc.contributor.authorPetković, Stojanen_US
dc.date.accessioned2019-09-23T10:23:55Z-
dc.date.available2019-09-23T10:23:55Z-
dc.date.issued2017-12-
dc.identifier.issn18751768en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/2817-
dc.description.abstract© 2017 Elsevier B.V. Recently, the interest of the forensic community has been focused on new Y-chromosomal short tandem repeats (Y-STRs), termed Rapidly Mutating Y-STRs (RM-YSTRs), which is able to differentiate between close males belonging to the same paternal lineage due to their high mutation rates. In this study, we have estimated a mutation rate for 13 RM-YSTR in 85 pairs of male relatives in the population of Serbia. We analysed 74 father-son pairs, and 11 twin pairs, to evaluate the capacity of distinguishing between male subjects within a single lineage. Each father-son couple was previously confirmed by autosomal STRs testing (AmpFℓSTR® Identifiler Plus™ kit, Applied Biosystems) with paternity probability ≥99.99% and also confirmed monozygotic or dizygotic twins. Results showed that, in the 74 father-son pairs 23 mutations were detected of which 22 were one-step mutations and 1 was two-step mutation, while in the 11 twin pairs 1 mutation was observed in one dizygotic twin pair. Five father-son pairs were found to have mutations at two loci, while one pair at four loci. Overall, the most mutable markers were DYF399S1, DYF387S1, DYF403S1a and DYS612. Our findings are encouraging and concur with previous studies showing that by RM-YSTR typing the discrimination power of male relatives could be considerably increased in comparison to every YSTR markers commonly used in forensic genetics.en_US
dc.language.isoenen_US
dc.relation.ispartofForensic Science International: Genetics Supplement Seriesen_US
dc.subjectRapidly mutatingen_US
dc.subjectY chromosome STRen_US
dc.subjectHaplotypeen_US
dc.subjectMutationen_US
dc.subjectSerbiaen_US
dc.titleMutation rate at 13 rapidly mutating Y-STR loci in the population of Serbiaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1016/j.fsigss.2017.09.171-
dc.identifier.scopus2-s2.0-85030162574-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85030162574-
dc.description.versionPublisheden_US
dc.relation.lastpagee379en_US
dc.relation.firstpagee377en_US
dc.relation.volume6en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptMedicinski fakultet-
crisitem.author.deptKatedra za primenjene i inženjerske hemije-
crisitem.author.deptKatedra za sudsku medicinu-
crisitem.author.deptKatedra za sudsku medicinu-
crisitem.author.orcid0000-0002-2160-6023-
crisitem.author.parentorgUniverzitet u Novom Sadu-
crisitem.author.parentorgTehnološki fakultet-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
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