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2019 | 306 | 33-43

Article title

Walidacja wewnętrzna programu biostatystycznego LRmix Studio

Content

Title variants

EN
Internal validation of LRmix Studio biostatistical software

Languages of publication

Abstracts

EN
The source of DNA in a stain is never known with full certainty despite the fact that the evidential profile may match a DNA profile of a given person from the population. The statistical methods, including the likelihood ratio (LR) allow estimating the evidential power of the obtained result and assessing the ratio of the odds between competing hypotheses as to the origin of a DNA profile or mixture. Therefore using analyses based on probabilistic methods seems to be logically justified and allows reducing the subjectivism of interpretation of results. Thorough knowledge and understanding of the principles of operation and limitations of the tools used for statistical interpretation of the results of biological traces analyses in forensics is the key stage that precedes the formulation of conclusions. The process of checking the efficiency of LRmix Studio software as well as reliability and repeatability of results involved single profiles and mixtures from two and three persons. 1971 comparisons with referential profiles were performed. The correctness of generated conditional probabilities was determined and the limits, i.e. drop-outs number in the evidential profile whose exceeding might bring about false LR values were identified.
PL
Źródło pochodzenia DNA w śladzie nigdy nie jest znane z całą pewnością, mimo iż profil dowodowy może być zgodny z profilem DNA danej osoby z populacji. Metody statystyczne, w tym iloraz wiarygodności, pozwalają oszacować siłę dowodową uzyskanego wyniku oraz ocenić stosunek szans między konkurencyjnymi hipotezami, dotyczącymi pochodzenia profilu lub mieszaniny DNA. W rezultacie stosowanie analiz opartych na metodach probabilistycznych wydaje się logicznie uzasadnione oraz pozwala zmiejszyć subiektywizm w interpretacji wyników badań. Dokładne poznanie i zrozumienie zasad działania oraz ograniczeń narzędzi wykorzystywanych do statystycznych interpretacji wyników badań śladów biologicznych w kryminalistyce jest kluczowym etapem poprzedzającym formułowanie wniosków płynących z tych analiz. Proces sprawdzenia wydajności programu LRmix Studio oraz wiarygodności i powtarzalności wyników obejmował pojedyncze profile oraz mieszaniny od dwóch i trzech osób. Wykonano 1971 porównań z profilami referencyjnymi. Określono poprawność generowanych prawdopodobieństw warunkowych oraz wyznaczono ograniczenia w postaci liczby zjawisk drop-out w profilu dowodowym, których przekroczenie może generować fałszywe wartości LR.

Year

Issue

306

Pages

33-43

Physical description

Dates

published
2019

Contributors

  • Centralne Laboratorium Kryminalistyczne Policji
  • Centralne Laboratorium Kryminalistyczne Policji

References

  • Benschop, C.C.G., Van Der Beek, C.P., Meiland, H.C., Van Gorp, A.G.M., Westen, A.A., Sijen, T. (2011). Low template STR typing: Effect of replicate number and consensus method on genotyping reliability and DNA database search results. Forensic Science International: Genetics, 5(4), https://doi.org/10.1016/j.fsigen.2010.06.006.
  • Bleka, Ø., Benschop, C.C.G., Storvik, G., Gill, P. (2016). A comparative study of qualitative and quantitative models used to interpret complex STR DNA profiles. Forensic Science International: Genetics, 25, https://doi.org/10.1016/j.fsigen.2016.07.016.
  • Buckleton, J., Bright, J.A., Taylor, D. (2016). Forensic DNA evidence interpretation. W: J. Buckleton, J.A. Bright, D. Taylor (red.), Forensic DNA Evidence Interpretation. Boca Raton: CRC Press, https://doi.org/10.4324/9781315371115.
  • Coble, M.D., Buckleton, J., Butler, J.M., Egeland, T., Fimmers, R., Gill, P., ... Prinz, M. (2016). DNA Commission of the International Society for Forensic Genetics: Recommendations on the validation of software programs performing biostatistical calculations for forensic genetics applications. Forensic Science International: Genetics, 25, https:// doi.org/10.101/j.fsigen.2016.09.002.
  • ENFSI (2015). Best Practice Manual for the internal validation of probabilistic software to undertake DNA mixture interpretation (n.d.).
  • Gill, P., Buckleton, J. (2010). A universal strategy to interpret DNA profiles that does not require a definition of low-copy-number. Forensic Science International: Genetics, 4(4), https://doi.org/10.1016/j.fsigen.2009.09.008.
  • Gill, P., Gusmão, L., Haned, H., Mayr, W.R., Morling, N., Parson, W., ... Weir, B.S. (2012). 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 Science International: Genetics, 6(6), https://doi. org/10.1016/j.fsigen.2012.06.002.
  • Gill, P., Haned, H. (2013). A new methodological framework to interpret complex DNA profiles using likelihood ratios. Forensic Science International: Genetics, 7(2), https://doi.org/10.1016/j.fsigen.2012.11.002.
  • Gill, P., Whitaker, J., Flaxman, C., Brown, N., Buckleton, J. (2000). An investigation of the rigor of interpretation rules for STRs derived from less than 100 pg of DNA. Forensic Science International, 112(1), https://doi.org/10.1016/S0379-0738(00)00158-4.
  • Haned, H., Slooten, K., Gill, P. (2012). Exploratory data analysis for the interpretation of low template DNA mixtures. Forensic Science International: Genetics, 6(6), https://doi.org/10.1016/j.fsigen.2012.08.008.
  • Haned, H., Benschop, C.C.G., Gill, P D., Sijen, T. (2015). Complex DNA mixture analysis in a forensic context: Evaluating the probative value using a likelihood ratio model. Forensic Science International: Genetics, 16, https://doi.org/10.1016/j.fsigen. 2014.11.014.
  • Haned, H., Gill, P. (2011). Analysis of complex DNA mixtures using the Forensim package. Forensic Science International: Genetics Supplement Series, 3(1), https://doi.org/10.1016/j.fsigss.2011.08.039.
  • Haned, H., Jong, J. De. (2016). LRmix Studio 2.1 user manual. 1–21.
  • Moretti, T.R., Just, R.S., Kehl, S.C., Willis, L.E., Buckleton, J.S., Bright, J.A., ... Onorato, A.J. (2017). Internal validation of STRmixTM for the interpretation of single source and mixed DNA profiles. ForensicScience International: Genetics, 29, https://doi.org/10.1016/j.fsigen.2017.04.004.
  • Scientific Working Group on DNA Analysis Methods. (2016). Scientific Working Group on DNA Analysis Methods Validation Guidelines for DNA Analysis Methods SWGDAM Validation Guidelines for DNA Analysis Methods. (December 2016), https://docs.wixstatic.com/ugd/4344b0_813b241e8944497e 99b9c45b163b76bd.pdf.
  • Steffen, C.R., Coble, M.D., Gettings, K.B., Vallone, P.M. (2017). Corrigendum to ‘U.S. Population Data for 29 Autosomal STR Loci’ [Forensic Sci. Int. Genet. 7 (2013) e82e83](S1872497312002712) (10.1016/j.fsigen.2012.12.004). Forensic Science International: Genetics, 31, https://doi.org/10.1016/j.fsigen.2017.08.011
  • Taylor, D. (2014). Using continuous DNA interpretation methods to revisit likelihood ratio behaviour. Forensic Science International: Genetics, 11(1), https://doi.org/10.101/j.fsigen.2014.03.008.
  • Welch, L.A., Gill, P., Phillips, C., Ansell, R., Morling, N., Parson, W., ... Bastisch, I. (2012). European Network of Forensic Science Institutes (ENFSI): Evaluation of new commercial STR multiplexes that include the European Standard Set (ESS) of markers. Forensic Science International: Genetics, 6(6), https://doi. org/10.1016/j.fsigen.2012.03.005.
  • Yoon, J. H., Lee, C.S., O’Connor, T.R., Yasui, A., Pfeifer, G.P. (2000). The DNA damage spectrum produced by simulated sunlight. Journal of Molecular Biology, 299(3), https://doi.org/10.1006/jmbi. 2000.3771.

Document Type

Publication order reference

Identifiers

Biblioteka Nauki
2065737

YADDA identifier

bwmeta1.element.ojs-doi-10_34836_pk_2019_306_4
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