| Literature DB >> 29506869 |
Anastasia Aliferi1, Jim Thomson2, Andrew McDonald3, Vanessa Molin Paynter1, Steven Ferguson4, Des Vanhinsbergh5, Denise Syndercombe Court1, David Ballard6.
Abstract
A total of 3128 Y-STR profiles from three UK and one Irish population have been analysed with the PowerPlex Y23 system and are reported here. Instances of haplotype sharing between apparently unrelated individuals were identified and further investigated with the use of the 5 additional markers within the Yfiler Plus kit, resulting in a reduction by 76% in the number of shared haplotypes. Furthermore, Yfiler Plus was also employed to verify locus deletions and duplications observed in Y23 genotypes while inconsistencies between the two kits were sequenced, revealing underlying Y23 primer binding site mutations in loci DYS392 and DYS576. Finally, the mechanism behind a previously reported population specific peak shift observed in DYS481 in South Asian samples has been evaluated and further investigated in a novel case of this phenomenon seen in a Black British individual featuring a different flanking region mutation.Keywords: DYS392; DYS481; DYS576; Mobility shift; Powerplex Y23; UK; Variant alleles; YSTR; Yfiler Plus
Mesh:
Year: 2018 PMID: 29506869 DOI: 10.1016/j.fsigen.2018.02.018
Source DB: PubMed Journal: Forensic Sci Int Genet ISSN: 1872-4973 Impact factor: 4.882