Laboratory of Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.
Forensic Sci Int Genet. 2012 Dec;6(6):810-8. doi: 10.1016/j.fsigen.2012.03.004. Epub 2012 Apr 13.
We explore the applicability of second generation sequencing (SGS) to sequence multiplexed forensic STR amplicons, both in a single contributor sample as in multiple-person mixtures with different ratios. We compare the results of a commercial STR profiling kit (Applied Biosystems AmpFlSTR(®) Profiler Plus(®)), analyzed both with capillary electrophoresis and with Roche GS FLX sequencing. An easy to use open-source software pipeline is provided, chaining together the different steps needed to start the analysis from a GS FLX FASTA file, resulting in a FASTA file containing the called and quantified alleles present in the data. Sequencing of multiplexed STR amplicons using Roche GS FLX titanium technology is technically feasible but the technology is not ideal for this purpose. The fraction of full length reads is small and the homopolymer sequencing error rate is high. The pipeline compresses the homopolymers to a single base to avoid false results caused by these homopolymers. The qualitative and quantitative results from the SGS STR analysis pipeline are comparable to the electrophoresis method. Additionally, the SGS method provides extra information and is able to call allele subtypes based on STR sequences in a database. In mixed samples, all alleles were reported from individuals that contributed at least 10% to the mixture.
我们探索了第二代测序(SGS)在单一供体样本和不同比例的多人混合样本中对序列多重法医 STR 扩增子的适用性。我们比较了商业 STR 分析试剂盒(Applied Biosystems AmpFlSTR(®) Profiler Plus(®))的结果,分别使用毛细管电泳和罗氏 454 GS FLX 测序进行分析。我们提供了一个易于使用的开源软件管道,将从 GS FLX FASTA 文件开始进行分析的不同步骤串联在一起,生成一个包含数据中存在的已调用和定量等位基因的 FASTA 文件。使用罗氏 454 GS FLX 钛技术对多重 STR 扩增子进行测序在技术上是可行的,但该技术并不理想。全长读取的分数很小,并且重复序列测序错误率很高。该管道将重复序列压缩为单个碱基,以避免由于这些重复序列导致的假结果。SGS STR 分析管道的定性和定量结果与电泳方法相当。此外,SGS 方法提供了额外的信息,并能够根据数据库中的 STR 序列调用等位基因亚型。在混合样本中,所有等位基因均来自至少贡献 10%混合物的个体。