The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises:: organisation, results and perspectives

被引:67
作者
Parson, W
Brandstätter, A
Alonso, A
Brandt, N
Brinkmann, B
Carracedo, A
Corach, D
Froment, O
Furac, I
Grzybowski, T
Hedberg, K
Keyser-Tracqui, C
Kupiec, T
Lutz-Bonengel, S
Mevag, B
Ploski, R
Schmitter, H
Schneider, P
Syndercombe-Court, D
Sorensen, E
Thew, H
Tully, G
Scheithauer, R
机构
[1] Med Univ Innsbruck, Inst Legal Med, A-6020 Innsbruck, Austria
[2] Inst Nacl Toxicol, Minist Justice, Madrid, Spain
[3] Natl Inst Criminalist & Criminol, Brussels, Belgium
[4] Univ Munster, Inst Legal Med, Munster, Germany
[5] Fac Farm & Bioquim, Buenos Aires, DF, Argentina
[6] Inst Pathol & Genet, Gerspinnes, Belgium
[7] Univ Zagreb, Dept Forens Med, Zagreb, Croatia
[8] Med Univ Bydgoszcz, Inst Mol & Forens Genet, Bydgoszcz, Poland
[9] SKL, Natl Lab Forens Sci, Linkoeping, Sweden
[10] Inst Legal Med, Lab CODGENE, Strasbourg, France
[11] Inst Forens Res, Krakow, Poland
[12] Univ Freiburg, Inst Legal Med, Freiburg, Germany
[13] Univ Oslo, Inst Legal Med, Oslo, Norway
[14] Univ Warsaw, Dept Forens Med, Warsaw, Poland
[15] Bundeskriminalant Wiesbaden, Wiesbaden, Germany
[16] Johannes Gutenberg Univ Mainz, Inst Legal Med, Mainz, Germany
[17] Barts & London Queen Marys Sch Med & Dent, Dept Haematol, London, England
[18] Univ Copenhagen, Dept Forens Genet, Inst Forens Med, Copenhagen, Denmark
[19] Armed Forces DNA Identif Lab, Rockville, MD USA
[20] Forens Sci Serv Inc, Birmingham, W Midlands, England
关键词
mitochondrial DNA sequence analysis collaborative exercised; quality score sequence analysis; heteroplasmy; forensic;
D O I
10.1016/j.forsciint.2003.11.008
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
This paper presents an overview of the organisation and the results of the collaborative exercises (CE) of the European DNA Profiling (EDNAP) Group's mitochondrial DNA population database project (EMPOP). The aim of the collaborative exercises was to determine whether uniformity of mtDNA sequencing results could be achieved among different laboratories. These were asked to sequence either the complete mtDNA control region or the two hypervariable regions HVI (16024-16365) and HVII (73-340) from DNA extracts, buccal swabs or bloodstains, proceeding in accordance with the protocol and strategies used in each individual laboratory. The results of the collaborative exercises were employed to identify possible sources of errors that could arise during the analysis and interpretation of mtDNA profiles. These findings were taken as a basis to tentatively make suitable arrangements for the construction of a high quality mtDNA database. One hundred fifty mtDNA profiles were submitted to the evaluating laboratory, and disaccording profiles were classified into four groups corresponding to the source of error: clerical errors, sample mix-ups, contaminations and discrepancies with respect to the mtDNA nomenclature. Overall. 14 disaccording haplotypes (16 individual errors) were observed. The errors included 10 clerical errors. 3 interpretation problems, 2 cases of sample mix-up and 1 case of point heteroplasmic mixture, where the 2 sequencing reactions brought inconsistent base calls. This corresponds to an error rate of 10.7% in a virtual mtDNA database consisting of the collaborative exercise results. However, this estimate is still conservative compared to conclusions drawn by authors of meanwhile numerous publications critically reviewing published mtDNA Population databases. Our results and earlier published concerns strongly emphasize the need for appropriate safety regulations when mtDNA profiles are compiled for database purposes in order to accomplish the high standard required for mtDNA databases that are used in the forensic context. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:215 / 226
页数:12
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