Evaluation of massively parallel sequencing for forensic DNA methylation profiling

被引:0
作者
Richards, Rebecca [1 ,2 ]
Patel, Jayshree [2 ]
Stevenson, Kate [2 ]
Harbison, SallyAnn [2 ]
机构
[1] Univ Auckland, Sch Chem Sci, Forens Sci Programme, Auckland, New Zealand
[2] Inst Environm Sci & Res Ltd ESR, Private Bag 92021, Auckland, New Zealand
关键词
DNA methylation; forensic science; massively parallel sequencing; MELT CURVE ANALYSIS; MONOZYGOTIC TWINS; AGE PREDICTION; BODY-FLUID; INDEPENDENT VALIDATION; EPIGENETIC DIFFERENCES; HUMAN-POPULATIONS; IDENTICAL-TWINS; IGF2/H19; LOCUS; CPG MARKERS;
D O I
10.1002/elps.201800086
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Epigenetics is an emerging area of interest in forensic science. DNA methylation, a type of epigenetic modification, can be applied to chronological age estimation, identical twin differentiation and body fluid identification. However, there is not yet an agreed, established methodology for targeted detection and analysis of DNA methylation markers in forensic research. Recently, a massively parallel sequencing-based approach has been suggested. The use of massively parallel sequencing is well established in clinical epigenetics and is emerging as a new technology in the forensic field. This review investigates the potential benefits, limitations, and considerations of this technique for the analysis of DNA methylation in a forensic context. The importance of a robust protocol, regardless of the methodology used, which minimizes potential sources of bias is highlighted.
引用
收藏
页码:2798 / 2805
页数:8
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