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面向欧洲的新型多路复用器——战略发展的修订与澄清

New multiplexes for Europe-amendments and clarification of strategic development.

作者信息

Gill Peter, Fereday Lyn, Morling Niels, Schneider Peter M

出版信息

Forensic Sci Int. 2006 Nov 10;163(1-2):155-7. doi: 10.1016/j.forsciint.2005.11.025. Epub 2006 Jan 19.

Abstract

Recently, the ENFSI/EDNAP groups issued advice on the design of the next generation of STR multiplexes in order to encourage standardisation within Europe. As the result of collaborative experimentation within the EDNAP group, we demonstrated that the low molecular weight STRs had substantial benefits to detect degraded samples. We subsequently recommended adoption of three new mini-STR loci to improve the success rate of degraded DNA markers, concurrent with the reduction in size of the existing STR markers in current use. This also improves the discriminating power of the system which is important to improve the power of national DNA databases. Subsequent discussions have occurred with manufacturers and members of the ENFSI/EDNAP groups. Because significant time and investment is required to develop new multiplexes of 13+ STR loci, manufacturers indicated that it would be preferable to adopt a staged approach. Two differing, but parallel strategies have now emerged. The first strategy employs a 13 STR loci multiplex incorporating three mini-STRs into the current multiplex test. The second strategy employs a multiplex of six high molecular weight STRs (in current use), modified to provide smaller amplicons combined with an additional two loci of high discriminating power. Eventually, the two strategies will converge to provide a single multiplex of 15 STR loci. The process will be guided by the ENFSI/EDNAP groups.

摘要

最近,欧洲法医遗传学学会/欧洲DNA分型网络分析组(ENFSI/EDNAP)发布了关于下一代STR复合扩增体系设计的建议,以促进欧洲范围内的标准化。作为EDNAP小组合作实验的结果,我们证明了低分子量STR在检测降解样本方面具有显著优势。随后,我们建议采用三个新的微型STR基因座,以提高降解DNA标记的成功率,同时缩小目前使用的现有STR标记的大小。这也提高了系统的鉴别能力,这对于提高国家DNA数据库的效能很重要。随后与制造商以及ENFSI/EDNAP小组的成员进行了讨论。由于开发13个以上STR基因座的新复合扩增体系需要大量时间和投资,制造商表示采用分阶段方法更为可取。现在出现了两种不同但并行的策略。第一种策略采用一个包含三个微型STR的13个STR基因座复合扩增体系,将其纳入当前的复合扩增检测中。第二种策略采用一个由六个高分子量STR(目前正在使用)组成的复合扩增体系,对其进行修改以提供更小的扩增子,并结合另外两个具有高鉴别力的基因座。最终,这两种策略将合并为一个包含15个STR基因座的复合扩增体系。该过程将由ENFSI/EDNAP小组指导。

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