Evidence map›Paper›PMID 30458020›Full record

ArticlePloS one2018

Four model variants within a continuous forensic DNA mixture interpretation framework: Effects on evidential inference and reporting.

Harish Swaminathan, Muhammad O Qureshi, Catherine M Grgicak, Ken Duffy, Desmond S Lun

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Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Interpol review of forensic biology and forensic DNA typing 2016-2019.Forensic science international. Synergy · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Harish SwaminathanDepartment of Anatomy & Neurobiology, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Muhammad O QureshiDepartment of Computer Science, Rutgers University, Camden, New Jersey, United States of America.
Catherine M GrgicakDepartment of Chemistry, Rutgers University, Camden, New Jersey, United States of America.
Ken DuffyHamilton Institute, Maynooth University, Kildare, Ireland.
Desmond S LunDepartment of Computer Science, Rutgers University, Camden, New Jersey, United States of America.ORCID 0000-0003-2276-2156

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Continuous mixture interpretation methods that employ probabilistic genotyping to compute the Likelihood Ratio (LR) utilize more information than threshold-based systems. The continuous interpretation schemes described in the literature, however, do not all use the same underlying probabilistic model and standards outlining which probabilistic models may or may not be implemented into casework do not exist; thus, it is the individual forensic laboratory or expert that decides which model and corresponding software program to implement. For countries, such as the United States, with an adversarial legal system, one can envision a scenario where two probabilistic models are used to present the weight of evidence, and two LRs are presented by two experts. Conversely, if no independent review of the evidence is requested, one expert using one model may present one LR as there is no standard or guideline requiring the uncertainty in the LR estimate be presented. The choice of model determines the underlying probability calculation, and changes to it can result in non-negligible differences in the reported LR or corresponding verbal categorization presented to the trier-of-fact. In this paper, we study the impact of model differences on the LR and on the corresponding verbal expression computed using four variants of a continuous mixture interpretation method. The four models were tested five times each on 101, 1-, 2- and 3-person experimental samples with known contributors. For each sample, LRs were computed using the known contributor as the person of interest. In all four models, intra-model variability increased with an increase in the number of contributors and with a decrease in the contributor's template mass. Inter-model variability in the associated verbal expression of the LR was observed in 32 of the 195 LRs used for comparison. Moreover, in 11 of these profiles there was a change from LR > 1 to LR < 1. These results indicate that modifications to existing continuous models do have the potential to significantly impact the final statistic, justifying the continuation of broad-based, large-scale, independent studies to quantify the limits of reliability and variability of existing forensically relevant systems.

Indexed as

AlgorithmsDNA FingerprintingForensic GeneticsHumansLikelihood FunctionsModels, StatisticalSoftwareUnited States

Identifiers

PMID30458020
PMCPMC6245789

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.