利用iScan系统上的全局筛选阵列开发验证Illumina Infinium检测,用于法医实验室

David A. Russell, Erin M. Gorden, Michelle A. Peck, Christina M. Neal, Mary C. Heaton, Jessica L. Bouchet, Alexander F. Koeppel, Elayna Ciuzio, Stephen D. Turner, Carmen R. Reedy
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引用次数: 1

摘要

微阵列处理技术可以在人类基因组中查询成千上万的单核苷酸多态性(snp),由于其在法医遗传家谱中的应用,最近在法医领域获得了关注,法医遗传家谱是基于对公共管理数据库中使用snp来比较远亲的分析,以发展调查线索或识别人类遗骸。迄今为止,还没有发表过使用DNA分析方法科学工作组(SWGDAM) DNA分析方法验证指南和联邦调查局质量保证标准对微阵列处理进行开发验证的文章。这些方法的验证是有必要的,以确定适合微阵列分析的样本,并在上传到家谱数据库之前评估获得的数据的质量。在本研究中,我们根据SWGDAM指南验证了Global Screening Array在法医调查中的应用,包括以下研究:精密度和准确性、灵敏度、污染、降解、物种特异性、模拟病例类型样本、混合物、可重复性和再现性以及稳定性。结果表明,在DNA输入低至0.20 ng时,SNP呼叫率>95%,准确的基因型呼叫。除了SNP调用率,我们还开发了信号强度和杂合度的解释阈值,以便对高度降解和/或非人类DNA进行样品质量评估和鉴定。该研究表明,可以从多种样本类型中生成高质量的数据,包括模拟法医悬案中经常遇到的挑战的模拟法医证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developmental Validation of the Illumina Infinium Assay Using the Global Screening Array on the iScan System for Use in Forensic Laboratories
Microarray processing, which interrogates hundreds of thousands of single nucleotide polymorphisms (SNPs) across the human genome, has recently gained traction in forensics due to its use in forensic genetic genealogy, which is based on analysis using SNPs to compare distant relatives in publicly curated databases for the purposes of developing investigative leads or identifying human remains. To date, there has been no published developmental validation of microarray processing using the Scientific Working Group on DNA Analysis Methods (SWGDAM) Validation Guidelines for DNA Analysis Methods and Federal Bureau of Investigation Quality Assurance Standards. Validation of these methods are warranted to identify samples suitable for microarray analysis and to assess the quality of the data obtained before upload to genealogical databases. In this study, we validated the Global Screening Array for use in forensic investigations according to SWGDAM guidelines, including the following studies: precision and accuracy, sensitivity, contamination, degradation, species specificity, mock case-type samples, mixtures, repeatability and reproducibility, and stability. Results indicated accurate genotype calls with SNP call rates >95% at DNA input as low as 0.20 ng. In addition to SNP call rate, we developed interpretation thresholds for signal intensity and heterozygosity to allow for sample quality assessment and identification of highly degraded and/or non-human DNA. This study demonstrates that high-quality data can be generated from multiple sample types, including mock forensic evidence that simulated the challenges that are often encountered in forensic cold cases.
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