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Ancient DNA Methods Improve Forensic DNA Profiling of Korean War and World War II Unknowns.

Zavala Elena I, EI Thomas, Jacqueline Tyler JT et al.

35052469 PubMed ID
19 Authors
2022-01-11 Published
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZE
Zavala Elena I
ET
EI Thomas
JT
Jacqueline Tyler JT
SK
Sturk-Andreaggi Kimberly
KD
K Daniels-Higginbotham
JJ
Jennifer J
MK
Meyers Kerriann K
KB
KK Barrit-Ross
SS
Suzanne S
AA
Aximu-Petri Ayinuer
AR
A Richter
JJ
Julia J
NB
Nickel Birgit
BB
B Berg
GE
Gregory E GE
MT
McMahon Timothy P
TM
TP Meyer
MM
Matthias M
MC
Marshall Charla
Chapter II

Abstract

Summary of the research findings

The integration of massively parallel sequencing (MPS) technology into forensic casework has been of particular benefit to the identification of unknown military service members. However, highly degraded or chemically treated skeletal remains often fail to provide usable DNA profiles, even with sensitive mitochondrial (mt) DNA capture and MPS methods. In parallel, the ancient DNA field has developed workflows specifically for degraded DNA, resulting in the successful recovery of nuclear DNA and mtDNA from skeletal remains as well as sediment over 100,000 years old. In this study we use a set of disinterred skeletal remains from the Korean War and World War II to test if ancient DNA extraction and library preparation methods improve forensic DNA profiling. We identified an ancient DNA extraction protocol that resulted in the recovery of significantly more human mtDNA fragments than protocols previously used in casework. In addition, utilizing single-stranded rather than double-stranded library preparation resulted in increased attainment of reportable mtDNA profiles. This study emphasizes that the combination of ancient DNA extraction and library preparation methods evaluated here increases the success rate of DNA profiling, and likelihood of identifying historical remains.

Chapter III

AI-Generated Summary

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Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

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