| Literature DB >> 34550443 |
Bowei Jiang1, Weifeng Qu2, Feng Wang1, Liming Zhang1, Haibo Rong1, Jienan Li2, Dan Wen2, Moutanou Modeste Judes Zeye2, Wei He2, Chudong Wang2, Hao Xing2, Tao Zhang1, Chuan Jin1, Li Chen1, Ying Liu2, Jifeng Cai2, Lagabaiyila Zha3.
Abstract
DNA profiling of short tandem repeats (STRs) is the primary method for genotyping forensic samples. However, degraded DNA and trace samples are still major problems for commercial 5- or 6-dye STR kits. In order to improve the performance of this method, we developed a novel 8-dye STR multiplex system containing 18 autosomal loci (D3S1358, D1S1656, TPOX, D16S539, vWA, D6S1043, D2S1338, CSF1PO, D19S433, D7S820, FGA, D8S1179, D5S818, D13S317, TH01, D21S11, D12S391, and PentaD) and the sex-determining locus Amelogenin, with all fragments smaller than 330 bases. Validation was carried out as recommended by the Scientific Working Group on DNA Analysis Methods. The results showed that complete profiles were obtainable when the input DNA was as low as 0.0625 ng. Full profiles were obtained even in the presence of inhibitors such as humic acid (< 300 ng/μl), hematin (< 100 μM), and indigo (0.01%). The 8-dye STR multiplex system also showed good performance in the detection degraded DNA samples. These results indicate that the 8-dye STR multiplex system is suitable for human DNA genotyping, including for difficult forensic materials.Entities:
Keywords: Developmental validation; GA118-24B genetic analyzer; STR; 8-dye STR multiplex system
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Year: 2021 PMID: 34550443 DOI: 10.1007/s00414-021-02695-9
Source DB: PubMed Journal: Int J Legal Med ISSN: 0937-9827 Impact factor: 2.686