A performance evaluation of Nextera XT and KAPA HyperPlus for rapid Illumina library preparation of long-range mitogenome amplicons. (July 2017)

• Record Type: Journal Article
• Authors: Ring, Joseph D.; Sturk-Andreaggi, Kimberly; Peck, Michelle A.; Marshall, Charla
• Is Part Of: Forensic science international. Volume 29(2017)
• Page Start: 174
• Page End: 180
• Publication Date: 2017-07
• Subjects: Mitochondrial DNA -- Next-generation sequencing (NGS) -- KAPA HyperPlus -- Nextera XT; Forensic genetics -- Periodicals; Génétique légale -- Périodiques; Forensic genetics; Electronic journals; Periodicals; 614.1
• DOI: 10.1016/j.fsigen.2017.04.003
• Languages: English
• ISSNs: 1872-4973

Abstract

Highlights: Nextera XT and HyperPlus were compared for mitogenome library preparation. Nextera XT libraries had areas of low coverage not observed in HyperPlus libraries. HyperPlus enabled uniform low-level variant detection across the mitogenome. Abstract: Next-generation sequencing (NGS) facilitates the rapid and high-throughput generation of human mitochondrial genome (mitogenome) data to build population and reference databases for forensic comparisons. To this end, long-range amplification provides an effective method of target enrichment that is amenable to library preparation assays employing DNA fragmentation. This study compared the Nextera XT DNA Library Preparation Kit (Illumina, San Diego, CA) and the KAPA HyperPlus Library Preparation Kit (Kapa Biosystems, Wilmington, MA) for enzymatic fragmentation and indexing of ∼8500 bp mitogenome amplicons for Illumina sequencing. The Nextera XT libraries produced low-coverage regions that were consistent across all samples, while the HyperPlus libraries resulted in uniformly high coverage across the mitogenome, even with reduced-volume reaction conditions. The balanced coverage observed from KAPA HyperPlus libraries enables not only low-level variant calling across the mitogenome but also increased sample multiplexing for greater processing efficiency.