Forensic evaluation of the Asia Pacific ancestry-informative MAPlex assay.


Journal

Forensic science international. Genetics
ISSN: 1878-0326
Titre abrégé: Forensic Sci Int Genet
Pays: Netherlands
ID NLM: 101317016

Informations de publication

Date de publication:
09 2020
Historique:
received: 19 02 2020
revised: 22 04 2020
accepted: 15 06 2020
pubmed: 3 7 2020
medline: 13 7 2021
entrez: 3 7 2020
Statut: ppublish

Résumé

DNA intelligence, and particularly the inference of biogeographical ancestry (BGA) is increasing in interest, and relevance within the forensic genetics community. The majority of current MPS-based forensic ancestry-informative assays focus on the differentiation of major global populations. The recently published MAPlex (Multiplex for the Asia Pacific) panel contains 144 SNPs and 20 microhaplotypes and aims to improve the differentiation of populations in the Asia Pacific region. This study reports the first forensic evaluation of the MAPlex panel using AmpliSeq technology and Ion S5 sequencing. This study reports on the overall performance of MAPlex including the assay's sequence coverage distribution and stability, baseline noise and description of problematic SNPs. Dilution series, artificially degraded and mixed DNA samples were also analysed to evaluate the sensitivity of the panel with challenging or compromised forensic samples. As the first panel to combine biallelic SNPs, multiple-allele SNPs and microhaplotypes, the MAPlex assay demonstrated an enhanced capacity for mixture detection, not easily performed with common binary SNPs. This performance evaluation indicates that MAPlex is a robust, stable and highly sensitive assay that is applicable to forensic casework for the prediction of BGA.

Identifiants

pubmed: 32615397
pii: S1872-4973(20)30117-4
doi: 10.1016/j.fsigen.2020.102344
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102344

Subventions

Organisme : NHGRI NIH HHS
ID : UM1 HG008901
Pays : United States

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

C Xavier (C)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: catarina.gomes@i-med.ac.at.

M de la Puente (M)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria; Forensic Genetics Unit, Institute of Forensic Sciences, University of Santiago de Compostela, Spain.

C Phillips (C)

Forensic Genetics Unit, Institute of Forensic Sciences, University of Santiago de Compostela, Spain.

M Eduardoff (M)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.

A Heidegger (A)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.

A Mosquera-Miguel (A)

Forensic Genetics Unit, Institute of Forensic Sciences, University of Santiago de Compostela, Spain.

A Freire-Aradas (A)

Forensic Genetics Unit, Institute of Forensic Sciences, University of Santiago de Compostela, Spain.

R Lagace (R)

Human Identification Group, Thermo Fisher Scientific, CA, USA.

S Wootton (S)

Human Identification Group, Thermo Fisher Scientific, CA, USA.

D Power (D)

Thermo Fisher Scientific, Victoria, Australia.

W Parson (W)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria; Forensic Science Program, The Pennsylvania State University, University Park, PA, USA.

M V Lareu (MV)

Forensic Genetics Unit, Institute of Forensic Sciences, University of Santiago de Compostela, Spain.

R Daniel (R)

Office of the Chief Forensic Scientist, Forensic Services Department, Victoria Police, Macleod, Australia; National Centre for Forensic Studies, Faculty of Science & Technology, University of Canberra, ACT, Australia.

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Classifications MeSH