Massively parallel sequencing-enabled mixture analysis of mitochondrial DNA samples
被引:0
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作者:
Jennifer D. Churchill
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机构:University of North Texas Health Science Center,Center for Human Identification
Jennifer D. Churchill
Monika Stoljarova
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机构:University of North Texas Health Science Center,Center for Human Identification
Monika Stoljarova
Jonathan L. King
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机构:University of North Texas Health Science Center,Center for Human Identification
Jonathan L. King
Bruce Budowle
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机构:University of North Texas Health Science Center,Center for Human Identification
Bruce Budowle
机构:
[1] University of North Texas Health Science Center,Center for Human Identification
[2] Tallinn University of Technology,Department of Chemistry and Biotechnology
[3] King Abdulaziz University,Center of Excellence in Genomic Medicine Research (CEGMR)
来源:
International Journal of Legal Medicine
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2018年
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132卷
关键词:
Mitochondrial DNA;
Mixtures;
Massively parallel sequencing;
Ion S5;
Ion PGM;
D O I:
暂无
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学科分类号:
摘要:
The mitochondrial genome has a number of characteristics that provide useful information to forensic investigations. Massively parallel sequencing (MPS) technologies offer improvements to the quantitative analysis of the mitochondrial genome, specifically the interpretation of mixed mitochondrial samples. Two-person mixtures with nuclear DNA ratios of 1:1, 5:1, 10:1, and 20:1 of individuals from different and similar phylogenetic backgrounds and three-person mixtures with nuclear DNA ratios of 1:1:1 and 5:1:1 were prepared using the Precision ID mtDNA Whole Genome Panel and Ion Chef, and sequenced on the Ion PGM or Ion S5 sequencer (Thermo Fisher Scientific, Waltham, MA, USA). These data were used to evaluate whether and to what degree MPS mixtures could be deconvolved. Analysis was effective in identifying the major contributor in each instance, while SNPs from the minor contributor’s haplotype only were identified in the 1:1, 5:1, and 10:1 two-person mixtures. While the major contributor was identified from the 5:1:1 mixture, analysis of the three-person mixtures was more complex, and the mixed haplotypes could not be completely parsed. These results indicate that mixed mitochondrial DNA samples may be interpreted with the use of MPS technologies.
机构:
Inst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New ZealandInst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New Zealand
England, Ryan
Curnow, Nicholas
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Inst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New ZealandInst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New Zealand
Curnow, Nicholas
Liu, Alex
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机构:
Inst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New Zealand
Univ Auckland, Dept Forens Sci, Sch Chem Sci, Auckland 1, New ZealandInst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New Zealand
Liu, Alex
Stacey, Janet
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机构:
Inst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New ZealandInst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New Zealand
Stacey, Janet
Harbison, SallyAnn
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机构:
Inst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New ZealandInst Environm Sci & Res Ltd, Private Bag 92021, Auckland 1142, New Zealand
机构:
Royal Liverpool Univ Hosp, St Pauls Eye Unit, Liverpool L7 8XP, EnglandUniv Liverpool, Inst Life Course & Med Sci, Dept Eye & Vis Sci, Liverpool L69 3BX, England
Cheeseman, Robert
Willoughby, Colin
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机构:
Univ Liverpool, Inst Life Course & Med Sci, Dept Eye & Vis Sci, Liverpool L69 3BX, England
Ulster Univ, Biomed Sci Res Inst, Genom Med, Coleraine BT52 1SA, North IrelandUniv Liverpool, Inst Life Course & Med Sci, Dept Eye & Vis Sci, Liverpool L69 3BX, England