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首页> 外文期刊>International Journal of Legal Medicine >Insertion–deletion polymorphisms—utilization on forensic analysis
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Insertion–deletion polymorphisms—utilization on forensic analysis

机译:插入-缺失多态性-在法医分析中的利用

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摘要

Insertion–deletion (INDEL) markers are very frequent in the human genome and present several advantages for population and forensic studies, such as low mutation rates, easy interpretation, small amplicons, easy genotyping, and the possibility of using multiplex PCR. The great adaptability of INDELs for amplification of low copy number or degraded DNA allows its using as an interesting platform of genetic identity by DNA in forensic cases. In the present study, we tested the ability of 48 diallelic INDEL markers on genotyping forensic samples collected from different biological samples related to criminal cases. Moreover, we evaluated the lowest DNA concentration with which there was amplification of all markers from each one of three indel-plex panels. When comparing the performances obtained by the indel-plex panels described in this study with results obtained using Identifiler® kit (Applied Biosystems) related to forensic samples, as well as to control samples with different concentrations of DNA, we observed superior efficiency on samples with low copy number or in the presence of inhibitors.
机译:插入-缺失(INDEL)标记在人类基因组中非常常见,为人群和法医研究提供了许多优势,例如低突变率,易于解释,小扩增子,易于基因分型以及使用多重PCR的可能性。 INDEL对低拷贝数或降解的DNA的扩增具有很大的适应性,可将其用作法医案例中DNA有趣的遗传同一性平台。在本研究中,我们测试了48种INDEL标记物对从与刑事案件有关的不同生物样本收集的法医样本进行基因分型的能力。此外,我们评估了最低的DNA浓度,可从三个indel-plex面板的每一个中扩增出所有标记。当将本研究中所述的indel-plex面板所获得的性能与使用Identifiler®试剂盒(Applied Biosystems)所获得的与法医样品以及对照样品(具有不同浓度的DNA)相关的结果进行比较时,我们观察到了拷贝数低或存在抑制剂。

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