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Evaluation of OpenArray™ as a Genotyping Method for Forensic DNA Phenotyping and Human Identification

机译:openArray™评估作为法医DNA表型和人体鉴定的基因分型方法

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摘要

A custom plate of OpenArray™ technology was evaluated to test 60 single-nucleotide polymorphisms (SNPs) validated for the prediction of eye color, hair color, and skin pigmentation, and for personal identification. The SNPs were selected from already validated subsets (Hirisplex-s, Precision ID Identity SNP Panel, and ForenSeq DNA Signature Prep Kit). The concordance rate and call rate for every SNP were calculated by analyzing 314 sequenced DNA samples. The sensitivity of the assay was assessed by preparing a dilution series of 10.0, 5.0, 1.0, and 0.5 ng. The OpenArray™ platform obtained an average call rate of 96.9% and a concordance rate near 99.8%. Sensitivity testing performed on serial dilutions demonstrated that a sample with 0.5 ng of total input DNA can be correctly typed. The profiles of the 19 SNPs selected for human identification reached a random match probability (RMP) of, on average, 10−8. An analysis of 21 examples of biological evidence from 8 individuals, that generated single short tandem repeat profiles during the routine workflow, demonstrated the applicability of this technology in real cases. Seventeen samples were correctly typed, revealing a call rate higher than 90%. Accordingly, the phenotype prediction revealed the same accuracy described in the corresponding validation data. Despite the reduced discrimination power of this system compared to STR based kits, the OpenArray™ System can be used to exclude suspects and prioritize samples for downstream analyses, providing well-established information about the prediction of eye color, hair color, and skin pigmentation. More studies will be needed for further validation of this technology and to consider the opportunity to implement this custom array with more SNPs to obtain a lower RMP and to include markers for studies of ancestry and lineage.
机译:评估了OpenArray™技术的定制板,以测试验证的60个单核苷酸多态性(SNP),用于预测眼睛颜色,毛发颜色和皮肤色素沉着,以及个人识别。 SNPS选自已验证的子集(HirisPlex-S,Precision ID ID Identity SNP面板和Forenseq DNA签名预备套件)。通过分析314测序的DNA样品来计算每个SNP的一致性速率和呼叫率。通过制备稀释系列10.0,5.0,1.0和0.5ng来评估测定的敏感性。 OpenArray™平台获得了96.9%的平均呼叫率,并一致率接近99.8%。在连续稀释液上进行的敏感性测试证明,可以正确地打字具有0.5ng总输入DNA的样品。为人类识别选择的19个SNP的轮廓达到了平均10-8的随机匹配概率(RMP)。分析来自8个个人的21个生物证据的例子,在常规工作流程期间产生单短串联重复型材,证明了该技术在实际情况下的适用性。将十七个样品正确键入,揭示高于90%的呼叫率。因此,表型预测揭示了相应验证数据中描述的相同的精度。尽管该系统的识别能力降低了与基于STR基于基于STR基于基于STR基于基于的试剂盒,但OpenArray™系统可用于排除嫌疑人并优先考虑下游分析的样本,提供有关眼睛颜色,毛发和皮肤色素沉着的预测的良好信息。需要更多的研究以进一步验证这项技术,并考虑使用更多SNPS实现此自定义阵列的机会,以获得较低的RMP,并包括用于研究祖先和血统的标记。

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