4.5 Article

Development of a new 26plex Y-STRs typing system for forensic application

期刊

FORENSIC SCIENCE INTERNATIONAL-GENETICS
卷 13, 期 -, 页码 112-120

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.fsigen.2014.06.015

关键词

Forensic science; Validation; Y-STR; DNA typing

资金

  1. National Natural Science Foundation of People's Republic of China [81302620, 81330073]
  2. National Key Technology Research & Development Program of the Ministry of Science and Technology of People's Republic of China [2012BAK16B01]

向作者/读者索取更多资源

In this study, 26plex Y-STRs typing system, including 17 Y-STRs (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393, DYS385ab, DYS437, DYS438, DYS439, DYS448, DYS456, DYS458, DYS635 and GATA H4) recommended as YHRD standard loci and nine new highly discriminating Y-STRs (DYS549, DYS643, DYS388, DYS570, DYS533, DYS576, DYS460, DYS481 and DYS449), was established with 5-dye fluorescences labelling. Developmental validation indicated that the 26plex Y-STRs typing system was reproducible, accurate, sensitive and robust. The sensitivity of the system was such that a full profile was obtainable even with 125 pg of male DNA. Specificity testing was demonstrated by the lack of cross-reactivity with a variety of commonly encountered animal species and bacteria. Also, the multiplex is suitable for mixture study. An average of above 97% of the minor alleles detected with the male/male mixture with 1: 3 and 3: 1 ratios, while an average of above 70% of the minor alleles detected with the male/male mixture with 1: 19 and 19: 1 ratios. Full profiles are consistently detected with 125 pg of male DNA, even in the presence of excessive amounts of female DNA. In addition, the whole PCR amplification of the 26 Y-STRs can finish in 1 h, making the multiplex system suitable for fast-detection. For the forensic evaluation of the multiplex system, 516 haplotypes were found among 517 unrelated males. HD of the multiplex system was 0.9999925 while DC was 0.9980658, which is suitable for forensic application. (C) 2014 Elsevier Ireland Ltd. All rights reserved.

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