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Part of the book series: Advances in Forensic Haemogenetics ((HAEMOGENETICS,volume 6))

Abstract

The analysis of Short Tandem Repeat polymorphisms is widely used as a method for human identification. There is a demand to combine several STR loci with high discrimination power for multiplex analysis. STR polymorphisms with few alleles (e.g.: TC11, F13A) do not have the discrimination power compared to STR-systems like SE33 (ACTBP2). SE33 has more than 30 alleles and thus the space for the combination with other STR loci in multiplex analysis is reduced. Therefore STR polymorphisms like FGA (HUMFIBRA) and D18S51 with about 15–20 alleles seem to be a good compromise.

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References

  • Berschick P, Henke J, Henke L (1995) Analysis of the Short Tandem Repeat polymorphism SE33: A new high resolution separation of SE33 by means of direct blotting electrophoresis. In: Bär W, Fiori A, Rossi U (eds) Advances in Forensic Haemogenetics 5, Springer, Berlion Heidelberg, New York, p 323–325

    Google Scholar 

  • Clark JM (1988) Novel non-template addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases. NAR 16, 9677–9686.

    Article  PubMed  CAS  Google Scholar 

  • Kimpton CP, Gill P, Walton A, Urquhart A, Millican ES, Adams M (1993) Automated DNA profiling employing multiplex amplification of short tandem repeat loci. PCR Methods Appl. 3, 13–22.

    PubMed  CAS  Google Scholar 

  • Straub RE, Speer MC, Luo Y, Rojas K, Overhauser J, Ott J Gilliam C (1993) A microsatellite genetic linkage map of human chromosome 18. Genomics 15, 48–56.

    Article  PubMed  CAS  Google Scholar 

  • Urquhart A, Oldroyd NJ, Kimpton CP, Gill P (1995) Highly discriminating heptaplex short tandem repeat PCR system for forensic identification. BioTechniques 18, 116–121.

    PubMed  CAS  Google Scholar 

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© 1996 Springer-Verlag Berlin Heidelberg

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Berschick, P., Reinhold, J. (1996). Analysis of the Short Tandem Repeat Polymorphism D18S51: Allele Frequencies and Sequence Studies. In: Carracedo, A., Brinkmann, B., Bär, W. (eds) 16th Congress of the International Society for Forensic Haemogenetics (Internationale Gesellschaft für forensische Hämogenetik e.V.), Santiago de Compostela, 12–16 September 1995. Advances in Forensic Haemogenetics, vol 6. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-80029-0_16

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  • DOI: https://doi.org/10.1007/978-3-642-80029-0_16

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-60492-1

  • Online ISBN: 978-3-642-80029-0

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