| Literature DB >> 23623014 |
Adil Laouina1, Sellama Nadifi, Redouane Boulouiz, Marzouk El Arji, Jalal Talbi, Brahim El Houate, Hakima Yahia, Faiza Chbel.
Abstract
Precise knowledge of mutation rate at Y-STRs loci is essential for a correct evaluation of typing results in forensic casework and specially kinship genetic studies. In this study, we have examined 252 confirmed and unrelated father/son sample pairs from Moroccan population using the 17 Y-STR markers DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393, DYS385a, DYS385b, DYS437, DYS438, DYS439, DYS448, DYS456, DYS458, DYS635, and Y-GATA-H4 of the AmpFlSTR Yfiler™ kit used in routine casework. We observed a total of 15 single repeat mutations between fathers and sons as mutational events. Nine mutations resulted in the gain of a repeat in the son and six resulted in a loss of a repeat. The average mutation rate in the studied sample is 3.5×10(-3) (95% CI 2-5.8×10(-3)). Furthermore, Y-STRs mutation occurrence seems to be 4 times more frequent than autosomal STRs mutation in this sample.Entities:
Keywords: AmpFlSTR Yfiler™; Moroccan; Mutational events; Y-STRs
Mesh:
Year: 2013 PMID: 23623014 DOI: 10.1016/j.legalmed.2013.03.003
Source DB: PubMed Journal: Leg Med (Tokyo) ISSN: 1344-6223 Impact factor: 1.376