Parson Walther, Niederstätter Harald, Lindinger Alexandra, Gill Peter
Institute of Legal Medicine, Innsbruck Medical University, Müllerstr. 44, 6020 Innsbruck, Austria.
Forensic Sci Int Genet. 2008 Jun;2(3):238-42. doi: 10.1016/j.fsigen.2007.12.004. Epub 2008 Feb 4.
The ENFSI (European Network of Forensic Science Institutes) DNA Working Group undertook a collaborative project on Y-STR typing of DNA mixture samples that were centrally prepared and thoroughly tested prior to the shipment. Four commercial Y-STR typing kits (Y-Filer, Applied Biosystems, Foster City, CA, USA; Argus Y Nonaplex, Biotype, Dresden, Germany; Powerplex Y, Promega, Madison, WI, USA; and DYSplex-3, SERAC, Bad Homburg, Germany) were used for the amplification of the mixture samples. The results of the study showed a striking inter-laboratory difference of kit performance as determined from the peak heights of the obtained Y-STR genotypes. Variation in quantity and quality of the shipped DNA can be excluded as reason for the observed differences because both samples and shipping conditions were found to be reproducible in an earlier study. The results suggest that in some cases a laboratory-specific optimization process is indicated to reach a comparable sensitivity for the analysis of minute amounts of DNA.
欧洲法医学研究所网络(ENFSI)DNA工作组开展了一个关于DNA混合样本Y-STR分型的合作项目,这些样本在装运前经过集中制备和全面测试。使用了四种商用Y-STR分型试剂盒(Y-Filer,美国应用生物系统公司,加利福尼亚州福斯特城;Argus Y Nonaplex,德国生物型公司,德累斯顿;Powerplex Y,美国普洛麦格公司,威斯康星州麦迪逊;以及DYSplex-3,德国SERAC公司,巴特洪堡)对混合样本进行扩增。研究结果显示,根据所获得的Y-STR基因型的峰高确定,试剂盒性能在实验室间存在显著差异。由于在早期研究中发现样本和运输条件均可重现,因此可以排除运输DNA的数量和质量变化是观察到的差异的原因。结果表明,在某些情况下,需要进行特定于实验室的优化过程,以达到对微量DNA分析的可比灵敏度。