PCR in Forensic Science: A Critical Review

被引:11
|
作者
Mcdonald, Caitlin [1 ]
Taylor, Duncan [1 ,2 ]
Linacre, Adrian [1 ]
机构
[1] Flinders Univ S Australia, Coll Sci & Engn, GPO Box 2100, Adelaide, SA 5001, Australia
[2] Forens Sci SA, GPO Box 2790, Adelaide, SA 5001, Australia
关键词
denaturation; annealing; DNA amplification; polymerase chain reaction; STR amplification; POLYMERASE-CHAIN-REACTION; DNA PROFILING SUCCESS; DEVELOPMENTAL VALIDATION; MITOCHONDRIAL-DNA; ENZYMATIC AMPLIFICATION; INHIBITION MECHANISMS; THERMUS-AQUATICUS; SEQUENCE-ANALYSIS; MULTIPLEX ASSAY; TOUCHDOWN PCR;
D O I
10.3390/genes15040438
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The polymerase chain reaction (PCR) has played a fundamental role in our understanding of the world, and has applications across a broad range of disciplines. The introduction of PCR into forensic science marked the beginning of a new era of DNA profiling. This era has pushed PCR to its limits and allowed genetic data to be generated from trace DNA. Trace samples contain very small amounts of degraded DNA associated with inhibitory compounds and ions. Despite significant development in the PCR process since it was first introduced, the challenges of profiling inhibited and degraded samples remain. This review examines the evolution of the PCR from its inception in the 1980s, through to its current application in forensic science. The driving factors behind PCR evolution for DNA profiling are discussed along with a critical comparison of cycling conditions used in commercial PCR kits. Newer PCR methods that are currently used in forensic practice and beyond are examined, and possible future directions of PCR for DNA profiling are evaluated.
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页数:22
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