Advertisement
Research Article| Volume 9, P47-54, March 2014

Download started.

Ok

Euroforgen-NoE collaborative exercise on LRmix to demonstrate standardization of the interpretation of complex DNA profiles

      Abstract

      There has been very little work published on the variation of reporting practices of mixtures between laboratories, but it has been previously demonstrated that there is little consistency. This is because there is no current uniformity of practice, so different laboratories will operate using different rules. The interpretation of mixtures is not solely a matter of using some software to provide ‘an answer’. An assessment of a case will usually begin with a consideration of the circumstances of a crime. Assumptions made about the numbers of contributors follow from an examination of the electropherogram(s) – and these may differ between the prosecution and the defence hypotheses. There may be a necessity to evaluate several sets of hypotheses for any given case if the circumstances are uncertain. Once the hypotheses are formulated, the mathematical analysis is complex and can only be accomplished by the use of specialist software. In order to obtain meaningful results, it is essential that scientists are trained, not only in the use of the software, but also in the methodology to understand the likelihood ratio concept that is used. The Euroforgen-NoE initiative has developed a training course that utilizes the LRmix program to carry out the calculations. This software encompasses the recommendations of the ISFG DNA commissions on mixture interpretation and is able to interpret samples that may come from two or more contributors and may also be partial profiles. Recently, eighteen different laboratories were trained in the methodology. Afterwards they were asked to independently analyze two different cases with partial mixture DNA evidence and to write a statement court-report. We show that by introducing a structured training programme, it is possible to demonstrate, for the first time, that a high degree of standardization, leading to uniformity of results can be achieved by participating laboratories.

      Keywords

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Forensic Science International: Genetics
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Gill P.
        • Brenner C.H.
        • Buckleton J.S.
        • Carracedo A.
        • Krawczak M.
        • Mayr W.R.
        • Morling N.
        • Prinz M.
        • Schneider P.M.
        • Weir B.S.
        DNA commission of the International Society of Forensic Genetics: Recommendations on the interpretation of mixtures.
        Forensic Sci. Int. 2006; 160: 90-101
        • Balding D.J.
        • Buckleton J.
        Interpreting low template DNA profiles.
        Forensic Sci. Int. Genet. 2009; 4: 1-10
        • Gill P.
        • Puch-Solis R.
        • Curran J.
        The low-template-DNA (stochastic) threshold-its determination relative to risk analysis for national DNA databases.
        Forensic Sci. Int. Genet. 2009; 3: 104-111
        • Haned H.
        • Egeland T.
        • Pontier D.
        • Pene L.
        • Gill P.
        Estimating drop-out probabilities in forensic DNA samples: a simulation approach to evaluate different models.
        Forensic Sci. Int. Genet. 2011; 5: 525-531
        • Mitchell A.A.
        • Tamariz J.
        • O‘Connell K.
        • Ducasse N.
        • Prinz M.
        • Caragine T.
        Likelihood ratio statistics for DNA mixtures allowing for drop-out and drop-in.
        Forensic Sci. Int. Genet. (Suppl. Ser.). 2011; 3: e240-e241
        • Tvedebrink T.
        • Eriksen P.S.
        • Asplund M.
        • Mogensen H.S.
        • Morling N.
        Allelic dropout probabilities estimated by logistic regression—further considerations and practical implementation.
        Forensic Sci. Int. Genet. 2012; 6: 263-267
        • Perlin M.W.
        • Sinelnikov A.
        An information gap in DNA evidence interpretation.
        PLoS One. 2009; 4: e8327
        • Gill P.
        • Haned H.
        A new methodological framework to interpret complex DNA profiles using likelihood ratios.
        Forensic Sci. Int. Genet. 2013; 7: 251-263
        • Gill P.
        • Gusmão L.
        • Haned H.
        • Mayr W.R.
        • Morling N.
        • Parson W.
        • Prieto L.
        • Prinz M.
        • Schneider H.
        • Schneider P.M.
        • Weir B.S.
        DNA commission of the International Society of Forensic Genetics: recommendations on the evaluation of STR typing results that may include drop-out and/or drop-in using probabilistic methods.
        Forensic Sci. Int. Genet. 2012; 6: 679-688
        • Gill P.
        • Whitaker J.
        • Flaxman C.
        • Brown N.
        • Buckleton J.
        An investigation of the rigor of interpretation rules f or STRs derived from less than 100 pg of DNA.
        Forensic Sci. Int. 2000; 112: 17-40
        • Benschop C.C.
        • van der Beek C.P.
        • Meiland H.C.
        • van Gorp A.G.
        • Westen A.A.
        • Sijen T.
        Low template STR typing: effect of replicate number and consensus method on genotyping reliability and DNA database search results.
        Forensic Sci. Int. Genet. 2011; 5: 316-328
        • Benschop C.C.
        • Haned H.
        • de Blaeij T.J.
        • Meulenbroek A.J.
        • Sijen T.
        Assessment of mock cases involving complex low template DNA mixtures: A descriptive study.
        Forensic Sci. Int. Genet. 2012; 6: 697-707
        • Haned H.
        • Slooten K.
        • Gill P.
        Exploratory data analysis for the interpretation of low template DNA mixtures.
        Forensic Sci. Int. Genet. 2012; 6: 762-774
        • Gill P.
        • Curran J.
        • Neumann C.
        • Kirkham A.
        • Clayton T.
        • Whitaker J.
        • Lambert J.
        Interpretation of complex DNA profiles using empirical models and a method to measure their robustness.
        Forensic Sci. Int. Genet. 2008; 2: 91-103
        • Curran J.
        Interpretation of repeat measurement DNA evidence allowing for multiple contributors and population substructure.
        Forensic Sci. Int. 2005; 148: 47-53
      1. http://www.cstl.nist.gov/strbase/interlab/MIX05/MIX05poster.pdf, march 2013.

      2. http://www.gep-isfg.org/es/comisiones-trabajo/ejercicio-colaborativo-ghepmix-2009/resultados-ejercicio-colaborativo-sobre-analisis.html, march 2013.

        • Duewer D.L.
        • Kliner M.C.
        • Redman J.W.
        • Butler J.M.
        NIST mixed stain study 3: signal intensity balance in commercial short tandem repeat multiplexes.
        Anal. Chem. 2004; 76: 6928-6934
        • Balding D.J.
        Weight-of-Evidence for Forensic DNA Profiles.
        John Wiley and Sons Ltd., 2005