Kit-dependent discrepancy in D16S539 and general considerations for database matches

Throughout the last decade more companies have been offering multiplex PCR kits for forensic STR typing. As a consequence, it has been demonstrated, that an observed genotype may unexpectedly vary at a single locus when different STR kits have been used. Analysing STR profiles which have to be enter...

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Hauptverfasser: Zajac, Barbara Karolina (VerfasserIn) , Zehner, Richard (VerfasserIn) , Scheiper, Stefanie (VerfasserIn) , Weissenberger, Melanie (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 20 February 2018
In: Forensic science international. Genetics
Year: 2018, Jahrgang: 34, Pages: 148-151
ISSN:1878-0326
DOI:10.1016/j.fsigen.2018.02.012
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.fsigen.2018.02.012
Verlag, lizenzpflichtig, Volltext: http://www.sciencedirect.com/science/article/pii/S1872497318301005
Volltext
Verfasserangaben:Barbara Karolina Zajac, Richard Zehner, Stefanie Scheiper, Melanie Weissenberger
Beschreibung
Zusammenfassung:Throughout the last decade more companies have been offering multiplex PCR kits for forensic STR typing. As a consequence, it has been demonstrated, that an observed genotype may unexpectedly vary at a single locus when different STR kits have been used. Analysing STR profiles which have to be entered in a national database, unknown or undetected primer binding site mutations, insertions or deletions within the flanking region of STR loci may hinder matches and therefore have far-reaching consequences. The current study is a further example indicating that sequence variations in flanking regions are a common problem within STR typing which should not be underestimated. A deletion of 16 nucleotides close to the primer binding site downstream of the repeat sequence resulted in deviant genotypes at the D16S539 locus according to different STR kits used.
Beschreibung:Gesehen am 11.03.2020
Beschreibung:Online Resource
ISSN:1878-0326
DOI:10.1016/j.fsigen.2018.02.012