Body fluid identification and assignment to donors using a targeted mRNA massively parallel sequencing approach - results of a second EUROFORGEN / EDNAP collaborative exercise.

Forensic science body fluid identification coding region SNPs (cSNPs) linear discriminant analysis (LDA) mRNA profiling massively parallel sequencing (MPS) partial least squares (PLS)

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:
03 2020
Historique:
received: 19 09 2019
revised: 19 11 2019
accepted: 21 11 2019
pubmed: 24 12 2019
medline: 2 2 2021
entrez: 24 12 2019
Statut: ppublish

Résumé

In a previous EUROFORGEN/EDNAP collaborative exercise, we tested two assays for targeted mRNA massively parallel sequencing for the identification of body fluids/tissues, optimized for the Illumina MiSeq/FGx and the Ion Torrent PGM/S5 platforms, respectively. The task of the second EUROFORGEN/EDNAP collaborative exercise was to analyze dried body fluid stains with two different multiplexes, the former Illumina 33plex mRNA panel for body fluid/tissue identification and a 35plex cSNP panel for assignment of body fluids/tissues to donors that was introduced in a proof-of-concept study recently. The coding region SNPs (cSNPs) are located within the body fluid specific mRNA transcripts and represent a direct link between the body fluid and the donor. We predicted the origin of the stains using a partial least squares discriminant analysis (PLS-DA) model, where most of the single source samples were correctly predicted. The mixed body fluid stains showed poorer results, however, at least one component was predicted correctly in most stains. The cSNP data demonstrated that coding region SNPs can give valuable information on linking body fluids/tissues with donors in mixed body fluid stains. However, due to the unfavorable performance of some cSNPs, the interpretation remains challenging. As a consequence, additional markers are needed to increase the discrimination power in each body fluid/tissue category.

Identifiants

pubmed: 31869731
pii: S1872-4973(19)30405-3
doi: 10.1016/j.fsigen.2019.102208
pii:
doi:

Substances chimiques

Genetic Markers 0
RNA, Messenger 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102208

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

S Ingold (S)

Zurich Institute of Forensic Medicine, University of Zurich, Switzerland.

G Dørum (G)

Zurich Institute of Forensic Medicine, University of Zurich, Switzerland.

E Hanson (E)

National Center for Forensic Science, University of Central Florida, Orlando, USA.

D Ballard (D)

King's Forensics, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London, UK.

A Berti (A)

Carabinieri Scientific Department of Rome - Genetic Unit, Rome, Italy.

K B Gettings (KB)

National Institute of Standards and Technology, Material Measurement Laboratory, Gaithersburg, MD, United States.

F Giangasparo (F)

King's Forensics, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London, UK.

M-L Kampmann (ML)

Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.

F-X Laurent (FX)

Laboratoire de Police Scientifique de Lyon, Institut National de Police Scientifique, F-69134, Ecully, France.

N Morling (N)

Section of Forensic Genetics, Department of Forensic Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.

W Parson (W)

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

C R Steffen (CR)

National Institute of Standards and Technology, Material Measurement Laboratory, Gaithersburg, MD, United States.

A Ulus (A)

Laboratoire de Police Scientifique de Lyon, Institut National de Police Scientifique, F-69134, Ecully, France.

M van den Berge (M)

Division of Biological Traces, Netherlands Forensic Institute, P.O. Box 24044, 2490 AA, The Hague, The Netherlands.

K J van der Gaag (KJ)

Division of Biological Traces, Netherlands Forensic Institute, P.O. Box 24044, 2490 AA, The Hague, The Netherlands.

V Verdoliva (V)

Carabinieri Scientific Department of Rome - Genetic Unit, Rome, Italy.

C Xavier (C)

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

J Ballantyne (J)

National Center for Forensic Science, University of Central Florida, Orlando, USA; Department of Chemistry, University of Central Florida, PO Box 162366, Orlando, FL 32816-2366, USA.

C Haas (C)

Zurich Institute of Forensic Medicine, University of Zurich, Switzerland. Electronic address: cordula.haas@irm.uzh.ch.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C

Classifications MeSH