High sensitivity multiplex short tandem repeat loci analyses with massively parallel sequencing. (May 2015)

• Record Type: Journal Article
• Authors: Zeng, Xiangpei; King, Jonathan L.; Stoljarova, Monika; Warshauer, David H.; LaRue, Bobby L.; Sajantila, Antti; Patel, Jaynish; Storts, Douglas R.; Budowle, Bruce
• Is Part Of: Forensic science international. Volume 16(2015:May)
• Page Start: 38
• Page End: 47
• Publication Date: 2015-05
• Subjects: Short tandem repeat (STR) -- Massively parallel sequencing (MPS) -- Illumina MiSeq; Forensic genetics -- Periodicals; Génétique légale -- Périodiques; Forensic genetics; Electronic journals; Periodicals; 614.1
• DOI: 10.1016/j.fsigen.2014.11.022
• Languages: English
• ISSNs: 1872-4973

Abstract

Highlights: Multiplex STR typing of 17 STRs and the Amelogenin locus is feasible by MPS. Sensitivity of detection is comparable with that of CE-based analyses A size selection method and quantity of amplified DNA necessary are described. The prototype STR multiplex and the illumina MiSeq generated reliable DNA profiles. Intra-repeat SNPs were observed and this additional variation may be useful. Abstract: STR typing in forensic genetics has been performed traditionally using capillary electrophoresis (CE). However, CE-based method has some limitations: a small number of STR loci can be used; stutter products, dye artifacts and low level alleles. Massively parallel sequencing (MPS) has been considered a viable technology in recent years allowing high-throughput coverage at a relatively affordable price. Some of the CE-based limitations may be overcome with the application of MPS. In this study, a prototype multiplex STR System (Promega) was amplified and prepared using the TruSeq DNA LT Sample Preparation Kit (Illumina) in 24 samples. Results showed that the MinElute PCR Purification Kit (Qiagen) was a better size selection method compared with recommended diluted bead mixtures. The library input sensitivity study showed that a wide range of amplicon product (6–200 ng) could be used for library preparation without apparent differences in the STR profile. PCR sensitivity study indicated that 62 pg may be minimum input amount for generating complete profiles. Reliability study results on 24 different individuals showed that high depth of coverage (DoC) and balanced heterozygote allele coverage ratios (ACRs) could be obtained with 250 pg of input DNA, and 62 pg could generate complete or nearly complete profiles. These studies indicate that this STR multiplex system and the Illumina MiSeq can generate reliable STR profiles at a sensitivity level that competes with current widely used CE-based method.