Evaluation of 13 short tandem repeat loci for use in personal identification applications
- PMID: 7912887
- PMCID: PMC1918216
Evaluation of 13 short tandem repeat loci for use in personal identification applications
Abstract
Personal identification by using DNA typing methodologies has been an issue in the popular and scientific press for several years. We present a PCR-based DNA-typing method using 13 unlinked short tandem repeat (STR) loci. Validation of the loci and methodology has been performed to meet standards set by the forensic community and the accrediting organization for parentage testing. Extensive statistical analysis has addressed the issues surrounding the presentation of "match" statistics. We have found STR loci to provide a rapid, sensitive, and reliable method of DNA typing for parentage testing, forensic identification, and medical diagnostics. Valid statistical analysis is generally simpler than similar analysis of RFLP-VNTR results and provides powerful statistical evidence of the low frequency of random multilocus genotype matching.
Comment in
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Allelic association between the HUMF13A01 (AAAG)n STR locus and a nearby two-base insertion/deletion polymorphic marker.Am J Hum Genet. 1995 Apr;56(4):1005-6. Am J Hum Genet. 1995. PMID: 7717390 Free PMC article. No abstract available.
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