Evidence map›Paper›PMID 41501187›Full record

ArticleInternational journal of legal medicine2026

Technical reliability of genotyping SNPs for forensic DNA phenotyping using SNaPshot- and MPS-based assays.

Annica Gosch, Katja Anslinger, Jana Naue

Abstract read
In one paragraph

Article in International journal of legal medicine, 2026. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Current state: Assessing DNA results considering transfer.Forensic science international. Synergy · 2026
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4 · The record

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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

3 authors.

Annica GoschInstitute of Legal Medicine, University Hospital of Cologne, Cologne, 50823, Germany.ORCID http://orcid.org/0000-0002-3315-7587
Katja AnslingerInstitute of Legal Medicine, LMU, Munich, 80336, Germany.
Jana NaueInstitute of Forensic Medicine, Medical Center- University of Freiburg, Freiburg, 79104, Germany. jana.naue@uniklinik-freiburg.de.ORCID http://orcid.org/0000-0001-9471-9013

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, several countries have undergone changes in their legal framework, now explicitly allowing the analysis of genetic markers for the purpose of forensic DNA phenotyping (FDP). Consequently, laboratory workflows for the analysis of appearance informative single nucleotide polymorphisms (SNPs) have been established in several laboratories. Currently, the HIrisPlex-S marker panel and webtool are the most widely used set of appearance informative SNP markers and statistical model used for phenotype predictions. However, many different laboratory protocols are employed for SNP genotyping, mostly using either massive parallel sequencing or single base extension technology. For the GEDNAP and TrACE proficiency tests, FDP modules were introduced in 2021 and 2023. These represented the first instances in which identical samples were analyzed by a fairly large number of laboratories, each of them employing their own laboratory-validated protocol. While mostly consistent phenotyping results were obtained, discrepant genotyping results were observed for some of the analyzed HIrisPlex-S-SNPs in BNC2, OCA2, and TYR. By performing a systematic in-silico analysis of commonly used primer sequences and sequencing the flanking regions of target SNPs in the affected samples from the collaborative exercises, we were able to identify primer binding site mutations, amplification of off-target products and overlap of SBE primers as risk factors for (analysis method-dependent) genotyping discrepancies. While the impact on phenotyping results was minor to negligible in all cases reported here, the issues uncovered by this in-depth analysis may provide a basis for improvements towards more consistent results in the future.

Indexed as

DNA FingerprintingGenotyping TechniquesHigh-Throughput Nucleotide SequencingPhenotypePolymorphism, Single NucleotideDNA PrimersForensic GeneticsGenetic MarkersGenotypeHumansReproducibility of ResultsSequence Analysis, DNADNA PrimersGenetic Markers

Identifiers

PMID41501187
PMCPMC13161349

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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.