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Human tandem repeat sequences in forensic DNA typing

By Keiji Tamaki and Alec J. Jeffreys

Abstract

This is the authors' final draft of the paper published as Legal Medicine, 2005, 7, pp.244-250. The definitive published version is available via www.sciencedirect.comIt has been twenty years since the first development of DNA fingerprinting and the start of forensic DNA typing. Ever since, human tandem repeat DNA sequences have been the main targets for forensic DNA analysis. These repeat sequences are classified into minisatellites (or VNTRs) and microsatellites (or STRs). In this brief review, we discuss the historical and current forensic applications of such tandem repeats

Publisher: Elsevier
Year: 2005
OAI identifier: oai:lra.le.ac.uk:2381/346

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Citations

  1. (2000). Allele diversity and germline mutation at the insulin minisatellite. Hum Mol Genet doi
  2. (2002). Allelic structures at hypervariable minisatellite B6.7 in Japanese show population specificity. doi
  3. Amplification of a variable number of tandem doi
  4. (1998). Different ancestor alleles: a reason for the bimodal fragment size distribution doi
  5. (2000). Distinguishing minisatellite mutation from non-paternity by MVR-PCR. Forensic Sci Int doi
  6. (1992). DNA technology in forensic science. doi
  7. (1999). Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7. Hum Mol Genet doi
  8. (1992). Forensic Sci doi
  9. (1999). Human minisatellites, repeat DNA instability and meiotic recombination. Electrophoresis. doi
  10. (1998). Influences of array size and homogeneity on minisatellite mutation. doi
  11. (1988). Isolation and mapping of a polymorphic DNA sequence (pMCT118) on chromosome 1p [D1S80]. Nucleic Acids Res doi
  12. (1994). Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism. doi
  13. (1988). Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. doi
  14. (2001). The application of minisatellite variant repeat mapping by PCR (MVR-PCR) in a paternity case showing false exclusion due to STR mutation. doi
  15. (1996). The evaluation of forensic DNA evidence. doi

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