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Research Article| Volume 16, P246-254, May 2015

DNA transfer by examination tools – a risk for forensic casework?

  • Bianca Szkuta
    Correspondence
    Corresponding author at: Office of the Chief Forensic Scientist, Victoria Police Forensic Services Department, 31 Forensic Drive, Macleod, Victoria 3085, Australia. Tel.: +61 9450 9736.
    Affiliations
    School of Life and Environmental Sciences, Deakin University, 75 Pigdons Road, Waurn Ponds, Victoria 3216, Australia

    Office of the Chief Forensic Scientist, Victoria Police Forensic Services Department, 31 Forensic Drive, Macleod, Victoria 3085, Australia
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  • Michelle L. Harvey
    Affiliations
    School of Life and Environmental Sciences, Deakin University, 75 Pigdons Road, Waurn Ponds, Victoria 3216, Australia
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  • Kaye N. Ballantyne
    Affiliations
    Office of the Chief Forensic Scientist, Victoria Police Forensic Services Department, 31 Forensic Drive, Macleod, Victoria 3085, Australia

    School of Psychological Sciences, La Trobe University, Bundoora, Victoria 3086, Australia
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  • Roland A.H. van Oorschot
    Affiliations
    Office of the Chief Forensic Scientist, Victoria Police Forensic Services Department, 31 Forensic Drive, Macleod, Victoria 3085, Australia
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Published:February 16, 2015DOI:https://doi.org/10.1016/j.fsigen.2015.02.004

      Highlights

      • The contamination risk of tools used during exhibit examination was evaluated.
      • Scissors, forceps and gloves are a contamination risk, they readily transfer DNA.
      • Transfer detectability is dependent on the substrates and biological sources involved.
      • Contaminating alleles may affect the probative value of DNA profiles in casework.

      Abstract

      The introduction of profiling systems with increased sensitivity has led to a concurrent increase in the risk of detecting contaminating DNA in forensic casework. To evaluate the contamination risk of tools used during exhibit examination we have assessed the occurrence and level of DNA transferred between mock casework exhibits, comprised of cotton or glass substrates, and high-risk vectors (scissors, forceps, and gloves). The subsequent impact of such transfer in the profiling of a target sample was also investigated. Dried blood or touch DNA, deposited on the primary substrate, was transferred via the vector to the secondary substrate, which was either DNA-free or contained a target sample (dried blood or touch DNA). Pairwise combinations of both heavy and light contact were applied by each vector in order to simulate various levels of contamination.
      The transfer of dried blood to DNA-free cotton was observed for all vectors and transfer scenarios, with transfer substantially lower when glass was the substrate. Overall touch DNA transferred less efficiently, with significantly lower transfer rates than blood when transferred to DNA-free cotton; the greatest transfer of touch DNA occurred between cotton and glass substrates. In the presence of a target sample, the detectability of transferred DNA decreased due to the presence of background DNA. Transfer had no impact on the detectability of the target profile, however, in casework scenarios where the suspect profiles are not known, profile interpretation becomes complicated by the addition of contaminating alleles and the probative value of the evidence may be affected. The results of this study reiterate the need for examiners to adhere to stringent laboratory cleaning protocols, particularly in the interest of contamination minimisation, and to reduce the handling of items to prevent intra-item transfer.

      Keywords

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