Volume 64, Issue 5 pp. 1312-1323
Paper

Extraction of DNA from Skeletonized Postcranial Remains: A Discussion of Protocols and Testing Modalities

Suni M. Edson M.S.

Corresponding Author

Suni M. Edson M.S.

Armed Forces DNA Identification Laboratory, Armed Forces Medical Examiner System, 115 Purple Heart Drive, Dover AFB, DE, 19902

College of Science and Engineering, Flinders University, Adelaide, South Australia, Australia

Corresponding author: Suni M. Edson, M.S. E-mail: [email protected]Search for more papers by this author
First published: 29 March 2019
Citations: 17
Presented in part at the 69th Annual Scientific Meeting of the American Academy of Forensic Sciences, February 13–18, 2017, in New Orleans, LA.
The opinions or assertions presented are the private views of the author and should not be construed as official or as reflecting the views of the Department of Defense, the Defense Health Agency, the Armed Forces Medical Examiner System, or the Defense POW/MIA Accounting Agency.

Abstract

This paper provides a retrospective of the DNA analysis performed by the Armed Forces Medical Examiner–Armed Forces DNA Identification Laboratory between 1990 and 2018. Over 13,000 postcranial osseous materials, comprised of wartime losses from World War II, the Korean War, and South-East Asia, were examined by the following: mitochondrial DNA sequencing, a modified AmpFlSTR® Yfiler™, AmpFlSTR® MiniFiler™, PowerPlex® Fusion, or NGS. Four different DNA extraction protocols were used: incomplete demineralization coupled with an organic purification; complete demineralization with an organic purification; complete demineralization with an inorganic purification using QIAquick PCR Purification Kit; and a protocol designed specifically for use with next-generation sequencing. In general, complete demineralization coupled with an organic purification was the optimal extraction protocol for sequencing of mitochondrial DNA, regardless of the osseous element tested. For STR testing, demineralization paired with an inorganic purification provided optimum results, regardless of kit used or osseous element tested.

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