Validation of the AMPFlSTR® MiniFilerTM PCR Amplification Kit for Use in Forensic Casework

被引:22
|
作者
Luce, Coral [1 ]
Montpetit, Shawn [2 ]
Gangitano, David [1 ]
O'Donnell, Patrick [2 ]
机构
[1] Sam Houston State Univ, Huntsville, TX 77340 USA
[2] San Diego Police Dept, San Diego, CA 92101 USA
关键词
forensic science; DNA typing; miniSTR; D13S317; D7S820; D2S1338; D21S11; D16S539; D18S51; CSF1PO; FGA; polymerase chain reaction; validation; AmpFlSTR; MINIPLEX PRIMER SETS; DEGRADED DNA; SKELETAL REMAINS; CONCORDANCE; SAMPLES; LOCI;
D O I
10.1111/j.1556-4029.2009.01099.x
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
The AmpFlSTR((R)) MiniFiler(TM) PCR Amplification Kit is designed to genotype degraded and/or inhibited DNA samples when the AmpFlSTR((R)) Identifiler(TM) PCR Amplification Kit is incapable of generating a complete genetic profile. Validation experiments, following the SWGDAM guidelines, were designed to evaluate the performance of MiniFiler. Data obtained demonstrated that MiniFiler, when used in conjunction with Identifiler, provided an increased ability to obtain genetic profiles from challenged samples. The optimum template range was found to be between 0.2 and 0.6 ng, with 0.3 ng yielding the best results. Full concordance was achieved between the MiniFiler kit and Identifiler kit except in a single case of a null allele at locus D21S11. Numerous instances of severe heterozygous peak imbalance (< 50%) were observed in single source samples amplified within the optimum range of input DNA suggesting that caution be taken when attempting to deduce component genotypes in a mixture.
引用
收藏
页码:1046 / 1054
页数:9
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