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DNA identification of compromised samples with massive parallel sequencing

Bibliographic Data

ID13119596
AuthorsAndreas Tillmar (0000-0001-9357-7658, Linköping University), Ida Grandell (Swedish National Board of Forensic Medicine), Kerstin Montelius (0000-0002-7525-7869, Swedish National Board of Forensic Medicine, corresponding author)
Year2018
Volume4
Issue4
Pages331-336
Publication date2018-10-29
Open AccessYes
TypeARTICLE
VenueForensic Sciences Research (JOURNAL)
Journal identifiersISSN: 2471-1411 • E-ISSN: 2096-1790
PublisherTaylor & Francis (PUBLISHER • GB)
DOI10.1080/20961790.2018.1509186
PMID32002491
OpenAlexW2899281443
LanguageEN
Citations received1
References cited27

Genetic profiling is a standard procedure for human identification, i.e. in criminal cases and mass disasters, and has been proven to be an important part in the process in the repatriation of victims to their relatives. In the event of a catastrophe whether it be a natural disaster, terror attack or accident, fatalities of many nationalities may be a consequence and international collaboration becomes necessary. Current DNA techniques used on a routine basis at forensic laboratories world-wide are very useful, and results reported from different labs are compared, making it possible to be matched in order to declare the identification of a victim. Statistical calculations of possibilities of a random match are achievable since population data from many parts of the world are available. However, decomposition and degradation of the remains are not uncommon in the aftermath of a catastrophe and hence it may be difficult to retrieve detailed DNA profiles from such samples. Massive parallel sequencing (MPS) is a technique capable of producing a vast amount of DNA sequence data in a high-through put manner, and panels of single nucleotide polymorphism (SNP) markers allow the amplification of small DNA fragments, often seen in compromised samples. Here, we report the results from a set of 10 samples from missing person identification cases, analyzed with an MPS based method comprising 131 SNP markers and compared with direct reference material or buccal swab samples collected from relatives of the deceased. We assess the weight of evidence of a match by statistical calculation. Furthermore, we compare results reported on different platforms using different SNP panels, and conclude that more work has to be done if results from missing person identification cases analyzed on MPS with SNP panels at different laboratories are to be fully reliable and thus comparable

Biology · Buccal swab · Computational biology · DNA · DNA profiling · DNA sequencing · Exome sequencing · Forensic identification · Gene · Identification (biology · Massive parallel sequencing · Mutation · Population · Computer Science · Environmental DNA in Biodiversity Studies · Forensic and Genetic Research · Genomics and Phylogenetic Studies · Medicine · Genetics

  • Modern advances in disaster victim identification

    Open Access•Peter Ellis•Forensic Sciences Research•2019

  • A global reference for human genetic variation

    Open Access•Corresponding authors, Adam Auton et al.•Nature•2015

Citations per year0.14
Citation span2019 - 2019 (1)
Highly citedNo

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