Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing
- PMID: 8434605
- PMCID: PMC1682118
Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing
Abstract
We have developed a new method for forensic identification of individuals, in which a panel of biallelic DNA markers are amplified by the PCR, and the variable nucleotides are detected in the amplified DNA fragments by the solid-phase minisequencing method. A panel of 12 common polymorphic nucleotides located on different chromosomes with reported allele frequencies close to .5 were chosen for the test. The allele frequencies for most of the markers were found to be similar in the Finnish and other Caucasian populations. We also introduce a novel approach for rapid determination of the population frequencies of biallelic markers. By this approach we were able to determine the allele frequencies of the markers in the Finnish population, by quantitative analysis of three pooled DNA samples representing 3,000 individuals. The power of discrimination and exclusion of the solid-phase minisequencing typing test with 12 markers was similar to that of three VNTR markers that are routinely used in forensic analyses at our institute. The solid-phase minisequencing method was successfully applied to type paternity and forensic case samples. We also show that the quantitative nature of our method allows typing of mixed samples.
Similar articles
-
Forensic DNA typing by the solid-phase minisequencing method.EXS. 1993;67:275-82. doi: 10.1007/978-3-0348-8583-6_25. EXS. 1993. PMID: 8400698
-
Amplification of reproducible allele markers for amplified fragment length polymorphism analysis.Biotechniques. 1992 Jan;12(1):16, 18, 20-2. Biotechniques. 1992. PMID: 1346500
-
Suitability of PCR methods for forensic investigation. Analysis of the 3'apoB VNTR system in an Italian population sample.Int J Legal Med. 1991;104(5):243-6. doi: 10.1007/BF01369577. Int J Legal Med. 1991. PMID: 1782142
-
[DNA analyses in forensic investigations].Lakartidningen. 1991 May 29;88(22):2055-9. Lakartidningen. 1991. PMID: 2051873 Review. Swedish.
-
Analysis and interpretation of mixed forensic stains using DNA STR profiling.Forensic Sci Int. 1998 Jan 9;91(1):55-70. doi: 10.1016/s0379-0738(97)00175-8. Forensic Sci Int. 1998. PMID: 9493345 Review.
Cited by
-
The Gln-Arg191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns.J Clin Invest. 1996 Aug 15;98(4):883-5. doi: 10.1172/JCI118869. J Clin Invest. 1996. PMID: 8770857 Free PMC article.
-
Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms.Nucleic Acids Res. 1994 Oct 11;22(20):4167-75. doi: 10.1093/nar/22.20.4167. Nucleic Acids Res. 1994. PMID: 7937143 Free PMC article.
-
Testing the feasibility of DNA typing for human identification by PCR and an oligonucleotide ligation assay.Am J Hum Genet. 1996 Jun;58(6):1239-46. Am J Hum Genet. 1996. PMID: 8651301 Free PMC article.
-
Delirium is a strong risk factor for dementia in the oldest-old: a population-based cohort study.Brain. 2012 Sep;135(Pt 9):2809-16. doi: 10.1093/brain/aws190. Epub 2012 Aug 9. Brain. 2012. PMID: 22879644 Free PMC article.
-
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L.Am J Hum Genet. 2002 Oct;71(4):863-76. doi: 10.1086/342773. Epub 2002 Sep 5. Am J Hum Genet. 2002. PMID: 12215968 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources