Institute of Forensic Medicine, University of Zurich, Zurich, Switzerland.
Wildlife Conservation Society, Zoological Health Program, Bronx, NY, USA.
Forensic Sci Int Genet. 2021 Jul;53:102493. doi: 10.1016/j.fsigen.2021.102493. Epub 2021 Mar 12.
Species identification of non-human biological evidence through DNA nucleotide sequencing is routinely used for forensic genetic analysis to support law enforcement. The gold standard for forensic genetics is conventional Sanger sequencing; however, this is gradually being replaced by high-throughput sequencing (HTS) approaches which can generate millions of individual reads in a single experiment. HTS sequencing, which now dominates molecular biology research, has already been demonstrated for use in a number of forensic genetic analysis applications, including species identification. However, the generation of HTS data to date requires expensive equipment and is cost-effective only when large numbers of samples are analysed simultaneously. The Oxford Nanopore Technologies (ONT) MinION™ is an affordable and small footprint DNA sequencing device with the potential to quickly deliver reliable and cost effective data. However, there has been no formal validation of forensic species identification using high-throughput (deep read) sequence data from the MinION making it currently impractical for many wildlife forensic end-users. Here, we present a MinION deep read sequence data validation study for species identification. First, we tested whether the clustering-based bioinformatics pipeline NGSpeciesID can be used to generate an accurate consensus sequence for species identification. Second, we systematically evaluated the read variation distribution around the generated consensus sequences to understand what confidence we have in the accuracy of the resulting consensus sequence and to determine how to interpret individual sample results. Finally, we investigated the impact of differences between the MinION consensus and Sanger control sequences on correct species identification to understand the ability and accuracy of the MinION consensus sequence to differentiate the true species from the next most similar species. This validation study establishes that ONT MinION sequence data used in conjunction with the NGSpeciesID pipeline can produce consensus DNA sequences of sufficient accuracy for forensic genetic species identification.
通过 DNA 核苷酸测序对非人类生物证据进行物种鉴定,通常用于法庭遗传学分析以支持执法。法庭遗传学的金标准是传统的 Sanger 测序;然而,这种方法正逐渐被高通量测序(HTS)方法所取代,后者可以在单次实验中生成数百万个个体读数。HTS 测序现在已经主导了分子生物学研究,已经在一些法庭遗传学分析应用中得到了证明,包括物种鉴定。然而,迄今为止,HTS 数据的生成需要昂贵的设备,只有在同时分析大量样本时才具有成本效益。牛津纳米孔技术(ONT)MinION™是一种经济实惠且占地面积小的 DNA 测序设备,具有快速提供可靠且具有成本效益的数据的潜力。然而,迄今为止,尚未使用 MinION 的高通量(深读)序列数据对法庭物种鉴定进行正式验证,这使得许多野生动物法庭鉴定最终用户目前无法使用它。在这里,我们展示了使用 MinION 深读序列数据进行物种鉴定的验证研究。首先,我们测试了基于聚类的生物信息学管道 NGSpeciesID 是否可用于生成用于物种鉴定的准确共识序列。其次,我们系统地评估了生成的共识序列周围的读变异分布,以了解我们对所得共识序列的准确性有多少信心,并确定如何解释单个样本结果。最后,我们研究了 MinION 共识序列与 Sanger 对照序列之间的差异对正确物种鉴定的影响,以了解 MinION 共识序列区分真实物种和下一个最相似物种的能力和准确性。这项验证研究表明,ONT MinION 序列数据与 NGSpeciesID 管道结合使用,可以生成足够准确的共识 DNA 序列,用于法庭遗传学物种鉴定。