| Literature DB >> 30915532 |
Yongsong Zhou1, Tong Xie1, Yuxin Guo2,3, Xinglin Mei4, Qiong Lan1, Yating Fang1, Xiaoye Jin2,3, Bofeng Zhu5,6,7.
Abstract
The Y chromosome short tandem repeat (Y-STR) haplotyping method has been widely used in forensic applications. However, the existing Y-STR panels are not the ideal tools for criminal investigation and database applications because of their relatively low discriminatory capacity (DC) or high mutation rates. In the present study, the multiplex PCR assay (AGCU Y30) for simultaneous amplification of 30 slowly and moderately mutated Y-STR loci labeled by 6-dye fluorescence was developed and validated. The AGCU Y30 assay was capable of amplification purified DNA from casework and database samples on FTA™ cards in direct amplification module with a 10 μL reaction volume. Furthermore, the genetic diversities and forensic parameters of AGCU Y30 were performed using 719 unrelated male samples, demonstrating its high level of genetic polymorphisms and DC in Nantong Han population. This validation study demonstrated good sensitivity, mixture samples, inhibitor tolerance, precision, and concordance for the AGCU Y30, which is suitable for forensic investigation and database construction.Keywords: AGCU Y30; Developmental validation; Forensic science; Y-STR
Year: 2019 PMID: 30915532 DOI: 10.1007/s00414-019-02037-w
Source DB: PubMed Journal: Int J Legal Med ISSN: 0937-9827 Impact factor: 2.686