Evidence map›Paper›PMID 37824042›Full record

ArticleForensic science, medicine, and pathology2024

Success rate of rapid DNA technology in kinship analysis for forensic purpose.

Tuğba Ünsal Sapan, Nasibe Yağmur Kartal, Şebnem Meherremli, Merve Erdem Obut, Kaan Yilancioğlu, Sevil Atasoy

Abstract read
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In one paragraph

Article in Forensic science, medicine, and pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 23% of its field
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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 1 institution in 2 countries.

Tuğba Ünsal SapanInstitute of Addiction and Forensic Sciences, Üsküdar University, Altunizade-Main Campus Üsküdar/Istanbul, 34662, Istanbul, Turkey. tugba.unsalsapan@uskudar.edu.tr.ORCID http://orcid.org/0000-0003-4744-2298
Nasibe Yağmur KartalInstitute of Addiction and Forensic Sciences, Üsküdar University, Altunizade-Main Campus Üsküdar/Istanbul, 34662, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-2272-5657
Şebnem MeherremliInstitute of Addiction and Forensic Sciences, Üsküdar University, Altunizade-Main Campus Üsküdar/Istanbul, 34662, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-2741-0056
Merve Erdem ObutInstitute of Addiction and Forensic Sciences, Üsküdar University, Altunizade-Main Campus Üsküdar/Istanbul, 34662, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-4837-2674
Kaan YilancioğluInstitute of Addiction and Forensic Sciences, Üsküdar University, Altunizade-Main Campus Üsküdar/Istanbul, 34662, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-0740-5580
Sevil AtasoyInstitute of Addiction and Forensic Sciences, Üsküdar University, Altunizade-Main Campus Üsküdar/Istanbul, 34662, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-0236-0267
Üsküdar University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reducing the time required for DNA analysis in forensic genetics can yield significant benefits, both in determining genealogical relationships for legal proceedings and in criminal cases. Swift identification of individuals plays a pivotal role in solving crimes and apprehending perpetrators. Additionally, in situations like mass disasters, prompt victim identification holds utmost importance. The Rapid DNA technology, introduced in 2012 to expedite DNA analysis, has evolved to streamline the process into a single step. This advancement not only minimizes the risk of human error and contamination, but also boasts a remarkable time advantage, delivering results in as little as 90 min. In this study, DNA profiles of 30 families (consisting of mothers, fathers, and children) were analyzed using the RapidHITTM ID System. The system automatically calculated maternity-paternity probabilities to assess the suitability of Rapid DNA technology for kinship analysis. For validation, DNA profiles were also generated using the 3500 GA method. The study revealed that 9 out of 30 families exhibited discrepancies in DNA profiling, leading to inaccuracies in automatic kinship analysis. Consequently, while the method offers rapid and user-friendly advantages for forensic sciences, the software underlying the system requires re-evaluation. Issues such as maternal-paternal exclusion in kinship analyses, arising from challenges like un-called alleles, warrant further attention.

Indexed as

DNA FingerprintingPaternityDNAFemaleForensic GeneticsHumansMaleMicrosatellite RepeatsPedigreePolymerase Chain ReactionTime FactorsDNADNA analysisForensic geneticsHuman identificationKinship analysesRapid DNA technologySTR

Identifiers

PMID37824042
OpenAlexW4387563989

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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.