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Cited by 183Forensic and Genetic ResearchGenetic diversity and population structureMolecular Biology Techniques and Applications

The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.

Evaluation of an automated DNA profiling system employing multiplex amplification of four tetrameric STR loci

Kimpton, Colin, Fisher, Deborah, Watson, Stephanie, Adams, Maia, Urquhart, Andy, Lygo, Joan, Gill, Peter·1994·International Journal of Legal Medicine

Abstract

We have examined the performance and reproducibility of an automated DNA profiling system which is based on the multiplex amplification of 4 tetrameric STR loci-HUMVWFA31/A. HUMTH01, HUMF13A1 and HUMFES/FPS. The system was able to type 100 pg of purified, undegraded, genomic DNA. At lower concentrations of DNA (below 100 pg), allelec drop-out occurred due to stochastic differences in allele copy number. Minor variation of individual PCR reagent concentrations or cycling temperatures did not result in a significant effect on the efficiency of amplification of any of the 4 loci in the quadruplex system. More substantial variation of reagent concentrations or cycling temperatures outside the optimum range of the system resulted in a reduction or complete loss of signal for one or more loci. This was also observed at high ionic strength or extreme pH. However, under all reagent concentrations and conditions studied, no artefact bands that could potentially result in the mistyping of a sample were apparent within the read region (130-240 bases) of the gel. Evaluation of both native and denaturing polyacrylamide gels revealed that, although native gels displayed faster run times, the sizing precision of such gels for certain STR loci was lower than that of denaturing gels. Also, artefact bands may be present within the read region of native gels. In conclusion the quadruplex amplification system described, coupled with automated fluorescence-based detection on denaturing polyacrylamide gels, appeared to be a robust and reliable system for individual identification.

Overview

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Crossref · 10.1007/bf01224776

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27 of 27 references verified0 citation errors · 0 not checkable

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Metadata

Authors
Kimpton, C., Fisher, D., Watson, S., Adams, M., Urquhart, A., Lygo, J., & Gill, P.
Affiliations
  • Armed Forces Institute of Pathology (US)
  • The Priory Hospital (GB)
Venue
International Journal of Legal Medicine
Published
1994-11
Volume
106
Issue
6
Pages
302-311
ISSN
  • 0044-3433 (ISSN-L)
  • 0937-9827
  • 1437-1596
OpenAlex
W2026896735
Cited by
183
References
27
Citations by year
2026: 1 · 2025: 4 · 2024: 8 · 2023: 2 · 2022: 7 · 2021: 3 · 2020: 8 · 2019: 3 · 2018: 4 · 2017: 2 · 2016: 1 · 2015: 2 · 2014: 3 · 2013: 2 · 2012: 2
FWCI
11.68
Type
journal article
Language
en
Open access
closed
Licence
www.springer.com/tdm (tdm)
Locations
  • International Journal of Legal Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Forensic and Genetic Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Molecular Biology Techniques and Applications
Keywords
DNA fingerprinting, multiplex PCR, HUMTH01, allele dropout, PCR artefacts, denaturing polyacrylamide gel electrophoresis, native polyacrylamide gel electrophoresis, individual identification, forensic genetics
MeSH terms
Alleles, Base Sequence, DNA, Electrophoresis, Polyacrylamide Gel, Evaluation Studies as Topic, Forensic Medicine, Humans, Hydrogen-Ion Concentration, Molecular Sequence Data, Multiphasic Screening, Osmolar Concentration, Repetitive Sequences, Nucleic Acid, Signal Processing, Computer-Assisted, Stochastic Processes, Temperature, Time Factors, Reproducibility of Results, Genome, Human, Bias, Polymerase Chain Reaction, DNA Fingerprinting

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