Evidence map›Paper›PMID 39833192›Full record

ArticleScientific reports2025

The impact of parameter variation in the quantification of forensic genetic evidence.

Camila Costa, Carolina Figueiredo, Sandra Costa, Paulo Miguel Ferreira, António Amorim, Lourdes Prieto, Nádia Pinto

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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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

7 authors.

Camila CostaDepartamento de Biologia, Faculdade de Ciências, Universidade do Porto, Porto, Portugal. camila75@live.com.pt.
Carolina FigueiredoDepartamento de Biologia, Faculdade de Ciências, Universidade do Porto, Porto, Portugal.
Sandra CostaBiologia, Laboratório de Polícia Científica da Polícia Judiciaria (LPC-PJ), Lisbon, Portugal.
Paulo Miguel FerreiraBiologia, Laboratório de Polícia Científica da Polícia Judiciaria (LPC-PJ), Lisbon, Portugal.
António AmorimDepartamento de Biologia, Faculdade de Ciências, Universidade do Porto, Porto, Portugal.
Lourdes PrietoGrupo de Medicina Xenómica, Instituto de Ciencias Forenses, Universidad de Santiago de Compostela, Santiago de Compostela, Spain.
Nádia Pintoi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.

Funding

Fundação para a Ciência e a Tecnologia 10.54499/2021.05655.BDFundação para a Ciência e a Tecnologia 2022.04997. CEECIND
6 · The paper itself

Abstract

Technological advancements have allowed the detection of increasingly complex forensic genetics samples, as minimum amounts of DNA can now be detected in crime scenes or other settings of interest. The weight of the evidence depends on several parameters regarding the population and sample-related analytical factors, the latter in a greater number when the DNA amount is considered. This led to the development of probabilistic genotyping software (PGS), able to deal with the associated complexities. This study aims to evaluate the impact on the evidence's weighing, when different analytical threshold values are used, and when different models and/or estimates for analytical artifacts, such as stutters or drop-in parameters, are considered. To reach this goal, three PGS, based on different statistical models, were used to analyze real casework pairs of samples composed of a mixture with either two or three estimated contributors, and a single-source sample associated. The obtained results show that the estimation of these parameters must not be overlooked, as they may considerably impact the outcome. This underlines the importance of proper parametrization in the analysis of forensic genetics identification problems when using complex samples, and the understanding by practitioners of how probabilistic genotyping informatics tools work to use them accurately.

Indexed as

DNAForensic GeneticsDNA FingerprintingGenotypeHumansModels, StatisticalSoftwareDNAAnalytical thresholdDrop-inForensic DNALikelihood ratioMixture samplesStutters

Identifiers

PMID39833192
PMCPMC11756398

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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.