Comparison of Reduced PCR Volume PowerPlex Fusion 6C Kit Validations on Manual and Automated Systems

Author:

Lőrincz Eszter É.1,Mátrai Norbert1ORCID,Rádóczy Katalin A.1,Cseppentő Tamás1,Magonyi Nóra M.1ORCID,Heinrich Attila1ORCID

Affiliation:

1. Department of Genetics, Hungarian Institute for Forensic Sciences, Mosonyi u. 9, 1087 Budapest, Hungary

Abstract

The PowerPlex Fusion 6C PCR™ amplification kit provides a strong discriminatory power for human identification. We have validated the kit with a reduced volume (12.5 µL) and as part of the validation we compared the efficiency of the polymerase chain reaction (PCR) prepared manually and on Hamilton Microlab® Autolys STAR Biorobot. Three years of casework data has been also included in the validation. Optimisation was carried out on different types of samples (blood, saliva, semen) and DNA was extracted robotically. Tests were conducted at two different cycle numbers (30;32), followed by analysis on both the Applied BiosystemsTM 3500 and 3500 xL Genetic Analyzer instruments (Applied Biosystems®, Foster City, CA, USA). When the PCR was prepared manually, no allele dropout was observed over 0.15 ng input DNA. Whereas when the PCR was prepared robotically, dropout already appeared at the level of 0.15 ng input DNA. In cases when increased cycle number was utilised, an increasing number of dropouts started to arise from 0.075 ng total input DNA. Despite the fact that robotically prepared PCR produced more missing alleles than the manually prepared PCR, using the optimal 0.5 ng input DNA, both methods proved to be reliable. Based on the results, our half-volume protocol is robust, and after three years of application it has proven to be effective with respect to a large number of casework samples.

Publisher

MDPI AG

Reference24 articles.

1. Developments in forensic DNA analysis;Haddrill;Emerg. Top Life Sci.,2021

2. Genotyping and interpretation of STR-DNA: Low-template, mixtures and database matches—Twenty years of research and development;Gill;Forensic Sci. Int. Genet.,2015

3. DNA fingerprinting in forensics: Past, present, future;Roewer;Investig. Genet,2013

4. Next generation sequencing: An application in forensic sciences?;Saiz;Ann. Hum. Biol.,2017

5. Analyzing population structure for forensic STR markers in next generation sequencing data;Aalbers;Genetics,2020

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