Literature DB >> 2032662

Report of a European collaborative exercise comparing DNA typing results using a single locus VNTR probe.

P M Schneider1, R Fimmers, S Woodroffe, D J Werrett, W Bär, B Brinkmann, B Eriksen, S Jones, A D Kloosterman, B Mevåg.   

Abstract

A collaborative exercise was carried out in 1989 among 12 European forensic laboratories using the single locus VNTR probe pYNH24, the restriction enzyme HinfI, the same set of human genomic DNA samples, and a standardized DNA size marker. The objectives of the exercise were: (1) to study the degree of variation within and between laboratories, (2) to obtain information on requirements for technical standardization allowing the exchange of typing results and (3) to compare different approaches for the identification of allelic DNA fragments of unknown size. Each laboratory carried out up to 10 independent typing experiments using the same DNA samples. The results were analysed independently by two laboratories using three different methods. The results of the exercise demonstrate the correlation of typing that can be achieved within and between laboratories under conditions of minimal standardization.

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Year:  1991        PMID: 2032662     DOI: 10.1016/0379-0738(91)90166-g

Source DB:  PubMed          Journal:  Forensic Sci Int        ISSN: 0379-0738            Impact factor:   2.395


  6 in total

1.  Population genetics and forensic efficiency data of 4 AMPFLP's.

Authors:  S Rand; C Puers; K Skowasch; P Wiegand; B Budowle; B Brinkmann
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

2.  Some technical parameters influencing the precision and accuracy of fragment size determination for RFLP's.

Authors:  C Puers; P Wiegand; B Brinkmann
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

3.  Semiparametric approach to match probability calculations using single locus probes.

Authors:  R Cao; J Alemany; C Cabrero; A Carracedo; A Díez; E Valverde
Journal:  Int J Legal Med       Date:  1996       Impact factor: 2.686

4.  Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array.

Authors:  R Andreassen; T Egeland; B Olaisen
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

5.  GEDNAP IV and V. The 4th and 5th Stain Blind Trials using DNA technology.

Authors:  P Wiegand; E Ambach; C Augustin; H Bratzke; U Cremer; J Edelmann; B Eriksen; U Germann; H Haas; L Henke
Journal:  Int J Legal Med       Date:  1995       Impact factor: 2.686

6.  Paternity testing with VNTR DNA systems. I. Matching criteria and population frequencies of the VNTR systems D2S44, D5S43, D7S21, D7S22, and D12S11 in Danes.

Authors:  N Morling; H E Hansen
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

  6 in total

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