Evidence map›Paper›PMID 40343479›Full record

ArticleInternational journal of legal medicine2025

The impact of considering different numbers of contributors in identification problems involving real casework mixture samples.

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

Abstract read
In one paragraph

Article in International journal of legal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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 CostaFaculdade de Ciências, Universidade Do Porto, Porto, Portugal. camilac@i3s.up.pt.ORCID http://orcid.org/0000-0002-8829-5581
Carolina FigueiredoFaculdade 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 AmorimFaculdade 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, R. Alfredo Allen 208, 4200 - 135, Porto, Portugal.

Funding

Fundação para a Ciência e a Tecnologia 10.54499/2021.05655.BDFundação para a Ciência e a Tecnologia 2022.04997. CEECINDFundação para a Ciência e a Tecnologia POCI-01-0145-FEDER-007274
6 · The paper itself

Abstract

Increasingly complex genetic samples are analyzed in forensic genetics routine, including mixtures to which more than one individual contributed. The standard problem relies on identification, aiming to quantify the likelihood of the donor of a reference sample being a contributor to the mixture. This is computed through a likelihood ratio (LR) and requires using devoted probabilistic genotyping software that may consider the quantity of the mixture's DNA (quantitative tools), beyond only the presence/absence of specific alleles (qualitative tools). In any case, the mixture's number of contributors (NoC) is a parameter that the user must introduce. Due to its nature, NoC is unknown for most real casework samples and needs to be estimated, which may be challenging due to poor DNA quality and quantity. This study aims to evaluate the impact of considering different NoC of real mixture samples (both over- and underestimating it after a first assessment of the expert) in identification problems through the pairwise comparison of LRs, using for the statistical assessment of both qualitative (LRmix Studio) and quantitative tools (EuroForMix and STRmix™). Different computational models showed different variations of the results, but for all, the impact was greater when considering a smaller NoC than the one initially estimated by the expert. Quantitative tools showed more sensitivity to NoC variation. Taking advantage of using real data, whose possible complexities surpass those of mock ones, this work highlights the impact that the NoC may have on the quantification of the proof, reinforcing the importance of its proper estimation.

Indexed as

DNADNA FingerprintingForensic GeneticsGenotypeHumansLikelihood FunctionsMicrosatellite RepeatsSoftwareDNAEstimationForensic DNALikelihood RatioNoCWeight-of-Evidence

Identifiers

PMID40343479
PMCPMC12354499

What OpenQuestion holds

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Registered trials

None linked

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.