Literature DB >> 24528595

Developmental validation of the PowerPlex(®) 21 System.

Martin G Ensenberger1, Carolyn R Hill2, Robert S McLaren3, Cynthia J Sprecher3, Douglas R Storts3.   

Abstract

The PowerPlex(®) 21 System is a STR multiplex that has been optimized for casework samples while still being capable of database workflows including direct amplification. The loci included in the multiplex offer increasing overlap with core loci used in different countries and regions throughout the world. The PowerPlex(®) 21 System contains D1S1656, D2S1338, D3S1358, D5S818, D6S1043, D7S820, D8S1179, D12S391, D13S317, D16S539, D18S51, D19S433, D21S11, Amelogenin, CSF1PO, FGA, Penta D, Penta E, TH01, TPOX, and vWA. These loci represent all 13 core CODIS loci in addition to loci commonly used in Asia and Europe. A developmental validation study was completed to document performance capabilities and limitations of the PowerPlex(®) 21 System. Data from this validation work served as the basis for the following conclusions: genotyping of single-source samples was reliable across a range of template DNA concentrations with >95% alleles called at 50 pg. Direct amplification of samples from FTA(®) storage cards was successfully performed using the reagents provided with the system and modified cycling protocols provided in the technical manual. Mixture analysis showed that over 95% of minor alleles were detected at 1:9 ratios. Reaction conditions including volume and annealing temperature as well as the concentrations of primers, DNA polymerase, magnesium, and Master Mix were shown to be optimal and able to withstand moderate variations without affecting system performance. Reproducible results were generated by different users at different sites. Finally, concordance studies showed consistent results when comparing the PowerPlex(®) 21 System with other commercially available STR-genotyping systems.
Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  CODIS; DNA typing; Forensic science; PowerPlex(®); Short tandem repeat (STR); Validation

Mesh:

Substances:

Year:  2013        PMID: 24528595     DOI: 10.1016/j.fsigen.2013.12.005

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  4 in total

1.  [Polymorphism analysis of 20 autosomal short-tandem repeat loci in southern Chinese Han population].

Authors:  Ling Chen; Hui-Jie Lu; Wei-An DU; Ping-Ming Qiu; Chao Liu
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2016-02-20

2.  Mutation analysis of 19 autosomal short tandem repeats in Chinese Han population from Shanghai.

Authors:  Chengchen Shao; Mingxi Lin; Zhihan Zhou; Yueqin Zhou; Yiwen Shen; Aimin Xue; Huaigu Zhou; Qiqun Tang; Jianhui Xie
Journal:  Int J Legal Med       Date:  2016-07-28       Impact factor: 2.686

3.  Collection and disinfection of forensic biological specimens in five cases concerning COVID-19 in Guangzhou, China.

Authors:  Xingyi Yang; Quyi Xu; Hong Liu; Jichao Xu; Dian Yang; Cheng Xiao; Huiying Hu; Yunyun Liu; Chao Liu
Journal:  Forensic Sci Int Synerg       Date:  2020-07-02

4.  Exploring STR sequencing for forensic DNA intelligence databasing using the Austrian National DNA Database as an example.

Authors:  Petra Hölzl-Müller; Martin Bodner; Burkhard Berger; Walther Parson
Journal:  Int J Legal Med       Date:  2021-08-26       Impact factor: 2.686

  4 in total

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