TY - JOUR
T1 - DNA Commission of the International Society for Forensic Genetics
T2 - Revised and extended guidelines for mitochondrial DNA typing
AU - Parson, W.
AU - Gusmão, L.
AU - Hares, D. R.
AU - Irwin, J. A.
AU - Mayr, W. R.
AU - Morling, N.
AU - Pokorak, E.
AU - Prinz, M.
AU - Salas, A.
AU - Schneider, P. M.
AU - Parsons, T. J.
N1 - Funding Information:
The research leading to this publication was funded in part by the Austrian Science Fund (FWF) [P22880-B12] and TR L397, as well as by the European Union Seventh Framework Programme ( FP7/2007-2013 ) under Grant Agreement No. 285487 (EUROFORGEN-NoE). It was also supported by Award No. 2011-MU-MU-K402 to Jodi A. Irwin, awarded by the National Institute of Justice, Office of Justice Programs, U.S. Department of Justice. The funding was administered by the American Registry of Pathology. Neither the U.S. Department of Justice nor the American Registry of Pathology had any role in study design; collection, analysis or interpretation of data; in the writing of this report; or in the decision to submit this paper for publication. A.S. received funding from the Ministerio de Ciencia e Innovación ( SAF2011-26983 ) and from the Xunta de Galicia ( EM 2012/045 ; Modalidad REDES: 2012-PG226). The authors would like to thank the staff of the Institute of Legal Medicine Innsbruck (GMI) for outstanding technical assistance throughout the past 15 years of EMPOP IT development, data generation and sequence review. We would like to thank Bettina Zimmermann and Gabriela Huber for collecting raw data for figural examples in this publication and Rebecca S. Just for useful discussions. Arne Dür (Institute of Mathematics, University of Innsbruck) and Alexander Röck are greatly acknowledged for the development of specific EMPOP software tools including SAM and EMMA.
PY - 2014/11
Y1 - 2014/11
N2 - The DNA Commission of the International Society of Forensic Genetics (ISFG) regularly publishes guidelines and recommendations concerning the application of DNA polymorphisms to the question of human identification. Previous recommendations published in 2000 addressed the analysis and interpretation of mitochondrial DNA (mtDNA) in forensic casework. While the foundations set forth in the earlier recommendations still apply, new approaches to the quality control, alignment and nomenclature of mitochondrial sequences, as well as the establishment of mtDNA reference population databases, have been developed. Here, we describe these developments and discuss their application to both mtDNA casework and mtDNA reference population databasing applications. While the generation of mtDNA for forensic casework has always been guided by specific standards, it is now well-established that data of the same quality are required for the mtDNA reference population data used to assess the statistical weight of the evidence. As a result, we introduce guidelines regarding sequence generation, as well as quality control measures based on the known worldwide mtDNA phylogeny, that can be applied to ensure the highest quality population data possible. For both casework and reference population databasing applications, the alignment and nomenclature of haplotypes is revised here and the phylogenetic alignment proffered as acceptable standard. In addition, the interpretation of heteroplasmy in the forensic context is updated, and the utility of alignment-free database searches for unbiased probability estimates is highlighted. Finally, we discuss statistical issues and define minimal standards for mtDNA database searches.
AB - The DNA Commission of the International Society of Forensic Genetics (ISFG) regularly publishes guidelines and recommendations concerning the application of DNA polymorphisms to the question of human identification. Previous recommendations published in 2000 addressed the analysis and interpretation of mitochondrial DNA (mtDNA) in forensic casework. While the foundations set forth in the earlier recommendations still apply, new approaches to the quality control, alignment and nomenclature of mitochondrial sequences, as well as the establishment of mtDNA reference population databases, have been developed. Here, we describe these developments and discuss their application to both mtDNA casework and mtDNA reference population databasing applications. While the generation of mtDNA for forensic casework has always been guided by specific standards, it is now well-established that data of the same quality are required for the mtDNA reference population data used to assess the statistical weight of the evidence. As a result, we introduce guidelines regarding sequence generation, as well as quality control measures based on the known worldwide mtDNA phylogeny, that can be applied to ensure the highest quality population data possible. For both casework and reference population databasing applications, the alignment and nomenclature of haplotypes is revised here and the phylogenetic alignment proffered as acceptable standard. In addition, the interpretation of heteroplasmy in the forensic context is updated, and the utility of alignment-free database searches for unbiased probability estimates is highlighted. Finally, we discuss statistical issues and define minimal standards for mtDNA database searches.
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U2 - 10.1016/j.fsigen.2014.07.010
DO - 10.1016/j.fsigen.2014.07.010
M3 - Article
C2 - 25117402
AN - SCOPUS:84907343169
SN - 1872-4973
VL - 13
SP - 134
EP - 142
JO - Forensic Science International: Genetics
JF - Forensic Science International: Genetics
ER -