A top-down approach to DNA mixtures.
DNA mixtures
Deconvolution
Likelihood ratios
Semi-continuous model
Weight of evidence
Journal
Forensic science international. Genetics
ISSN: 1878-0326
Titre abrégé: Forensic Sci Int Genet
Pays: Netherlands
ID NLM: 101317016
Informations de publication
Date de publication:
05 2020
05 2020
Historique:
received:
14
06
2019
revised:
23
12
2019
accepted:
16
01
2020
pubmed:
15
3
2020
medline:
23
3
2021
entrez:
15
3
2020
Statut:
ppublish
Résumé
Presently, there exist many different models and algorithms for determining, in the form of a likelihood ratio, whether there is evidence that a person of interest contributed to a mixed trace profile. These methods have in common that they model the whole trace, hence all its contributors, which leads to the computation time being mostly determined by the number of contributors that is assumed. At some point, these calculations are no longer feasible. We present another approach, in which we target the contributors of the mixture in the order of their contribution. With this approach the calculation time now depends on how many contributors are queried. This means that any trace can be subjected to calculations of likelihood ratios in favor of being a relatively prominent contributor, and we can choose not to query it for all its contributors, e.g., if that is computationally not feasible, or not relevant for the case. We do so without using a quantitative peak height model, i.e., we do not define a peak height distribution. Instead, we work with subprofiles derived from the full trace profile, carrying out likelihood ratio calculations on these with a discrete method. This lack of modeling makes our method widely applicable. The results with our top-down method are slightly conservative with respect to the one of a continuous model, and more so as we query less and less prominent contributors. We present results on mixtures with known contributors and on research data, analyzing traces with plausibly 6 or more contributors. If a top-k of most prominent contributors is targeted, it is not necessary to know how many other contributors there are for LR calculations, and the more prominent the queried contributor is relatively to all others, the less the evidential value depends on the specifics of a chosen peak height model. For these contributors the qualitative statement that more input DNA leads to larger peaks suffices. The evidential value for a comparison with minor contributors on the other hand, potentially depends much more on the chosen model. We also conclude that a trace's complexity, as meaning its (in)ability to yield large LR's that are not too model-dependent, is not measured by its number of contributors; rather, it is the equality of contribution that makes it harder to obtain strong evidence.
Identifiants
pubmed: 32169810
pii: S1872-4973(20)30021-1
doi: 10.1016/j.fsigen.2020.102250
pii:
doi:
Substances chimiques
DNA
9007-49-2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
102250Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.