Literature DB >> 8434605

Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing.

A C Syvänen1, A Sajantila, M Lukka.   

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.

Mesh:

Substances:

Year:  1993        PMID: 8434605      PMCID: PMC1682118     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  53 in total

1.  G to A polymorphism in the second exon of the BCL2 gene.

Authors:  S Tanaka; J Kant; J C Reed
Journal:  Nucleic Acids Res       Date:  1991-04-25       Impact factor: 16.971

2.  Phosphoglucomutase (PGM1) subtypes in a Finnish population determined by isoelectric focusing in agarose gel.

Authors:  M Lukka; C Ehnholm; T Kuusi
Journal:  Hum Hered       Date:  1985       Impact factor: 0.444

3.  The gamma 1 and gamma 2 subunits of human liver alcohol dehydrogenase. cDNA structures, two amino acid replacements, and compatibility with changes in the enzymatic properties.

Authors:  J O Höög; L O Hedén; K Larsson; H Jörnvall; H von Bahr-Lindström
Journal:  Eur J Biochem       Date:  1986-09-01

4.  Hypervariable 'minisatellite' regions in human DNA.

Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

5.  Group-specific component (Gc): subtypes in the Finnish population. Description of a new allele and an apparent mother-child incompatibility.

Authors:  M Lukka; P Turunen; M Kataja; C Ehnholm
Journal:  Hum Hered       Date:  1986       Impact factor: 0.444

6.  Production of interferon in human leukocytes from normal donors with the use of Sendai virus.

Authors:  K Cantell; S Hirvonen; H L Kauppinen; G Myllylä
Journal:  Methods Enzymol       Date:  1981       Impact factor: 1.600

7.  Analysis of the structure, transcripts, and protein products of bcl-2, the gene involved in human follicular lymphoma.

Authors:  Y Tsujimoto; C M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

8.  Two polymorphisms in the human lipoprotein lipase (LPL) gene.

Authors:  K L Fisher; G A FitzGerald; R M Lawn
Journal:  Nucleic Acids Res       Date:  1987-09-25       Impact factor: 16.971

9.  Complete protein sequence and identification of structural domains of human apolipoprotein B.

Authors:  T J Knott; R J Pease; L M Powell; S C Wallis; S C Rall; T L Innerarity; B Blackhart; W H Taylor; Y Marcel; R Milne
Journal:  Nature       Date:  1986 Oct 23-29       Impact factor: 49.962

10.  Molecular cloning of a human prion protein cDNA.

Authors:  H A Kretzschmar; L E Stowring; D Westaway; W H Stubblebine; S B Prusiner; S J Dearmond
Journal:  DNA       Date:  1986-08
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  40 in total

1.  High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR.

Authors:  S Germer; M J Holland; R Higuchi
Journal:  Genome Res       Date:  2000-02       Impact factor: 9.043

2.  Quantitative analysis of human DNA sequences by PCR and solid-phase minisequencing.

Authors:  A Suomalainen; A C Syvänen
Journal:  Mol Biotechnol       Date:  2000-06       Impact factor: 2.695

3.  Multiplex Pyrosequencing.

Authors:  Nader Pourmand; Elahe Elahi; Ronald W Davis; Mostafa Ronaghi
Journal:  Nucleic Acids Res       Date:  2002-04-01       Impact factor: 16.971

4.  Determination of single-nucleotide polymorphisms by real-time pyrophosphate DNA sequencing.

Authors:  A Alderborn; A Kristofferson; U Hammerling
Journal:  Genome Res       Date:  2000-08       Impact factor: 9.043

5.  Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA.

Authors:  Lovisa Lovmar; Mona Fredriksson; Ulrika Liljedahl; Snaevar Sigurdsson; Ann-Christine Syvänen
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

6.  A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer.

Authors:  Pia Vahteristo; Jirina Bartkova; Hannaleena Eerola; Kirsi Syrjäkoski; Salla Ojala; Outi Kilpivaara; Anitta Tamminen; Juha Kononen; Kristiina Aittomäki; Päivi Heikkilä; Kaija Holli; Carl Blomqvist; Jiri Bartek; Olli-P Kallioniemi; Heli Nevanlinna
Journal:  Am J Hum Genet       Date:  2002-07-28       Impact factor: 11.025

7.  Polymorphism ratio sequencing: a new approach for single nucleotide polymorphism discovery and genotyping.

Authors:  Robert G Blazej; Brian M Paegel; Richard A Mathies
Journal:  Genome Res       Date:  2003-02       Impact factor: 9.043

8.  SNP typing by apyrase-mediated allele-specific primer extension on DNA microarrays.

Authors:  Deirdre O'Meara; Afshin Ahmadian; Jacob Odeberg; Joakim Lundeberg
Journal:  Nucleic Acids Res       Date:  2002-08-01       Impact factor: 16.971

9.  CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.

Authors: 
Journal:  Am J Hum Genet       Date:  2004-04-30       Impact factor: 11.025

10.  Candidate SNPs for a universal individual identification panel.

Authors:  Andrew J Pakstis; William C Speed; Judith R Kidd; Kenneth K Kidd
Journal:  Hum Genet       Date:  2007-02-27       Impact factor: 4.132

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