ISO 17025 validation of a next-generation sequencing assay for relationship testing
Abstract
The HID‐Ion AmpliSeq™ Identity Panel is a next‐generation sequencing assay with 90 autosomal and 34 Y‐chromosome SNPs that are amplified in one PCR step and subsequently sequenced using the Ion Personal Genome Machine (Ion PGM™) System. This assay was validated for relationship testing in our ISO 17025 accredited laboratory in 2015. Here, the essential parts of the validation report submitted to the Danish Accreditation Fund are presented. A total of 100 unrelated Danes were typed in duplicates and the locus balance, heterozygote balance (Hb) and noise levels were analysed in detail. Two loci were disregarded for casework because genotyping was uncertain. Hb for rs7520386 was skewed and high levels of noise were observed in rs576261. Three general acceptance criteria for analysis of single‐source samples were defined: (i) sequencing depth > 200 reads, (ii) noise level < 3% and (iii) Hb > 0.3. A Python script named SNPonPGM was developed to assist the analyst by highlighting loci that do not fulfil the general acceptance criteria. Furthermore, SNPonPGM has functions that reduce the hands‐on time of the reporting officer to a few minutes per case. Mixtures with DNA from two individuals in a 1:24 ratio were readily identified using the three criteria and the SNPonPGM script.
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Laboratories seeking accreditation under CLIA or ISO 17025 must conduct positive and negative controls with every batch, document lot numbers, and participate in external proficiency testing.
“Laboratories seeking accreditation under CLIA or ISO 17025 [46] must conduct positive and negative controls with every batch, document lot numbers, and participate in external proficiency testing.”
From Genetic Insights into the Economic Toll of Cell Line Misidentification: A Comprehensive Review (2026) · cites this paper as [46]
Introducing such test systems must be critically validated under CLIA or ISO 17025 guidelines before becoming part of forensic assays.
“Moreover, introducing such test systems must be critically validated under these guidelines before becoming part of forensic assays [46].”
From Genetic Insights into the Economic Toll of Cell Line Misidentification: A Comprehensive Review (2026) · cites this paper as [46]
Cites
Phillips, C., García-Magariños, M., Salas, A., Carracedo, Á., & Lareu, M. V. (2012) · Transfusion Medicine and Hemotherapy · doi:10.1159/000338857 · Cited by 65 · see citing works
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Genetic Insights into the Economic Toll of Cell Line Misidentification: A Comprehensive Review
Weiskirchen, R. (2026) · Medical Sciences · doi:10.3390/medsci14010025 · Cited by 4 · see citing works
- Authors
- Buchard, A., Kampmann, M., Poulsen, L., Børsting, C., & Morling, N.
- Affiliations
- University of Copenhagen (DK)
- Corresponding author
- Buchard, Anders
- Venue
- ELECTROPHORESIS
- Publisher
- Wiley
- Published
- 2016-10
- Volume
- 37
- Issue
- 21
- Pages
- 2822-2831
- ISSN
- 0173-0835 (ISSN-L)
- 1522-2683
- OpenAlex
- W2530226004
- Cited by
- 64
- References
- 1
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 5 · 2023: 9 · 2022: 5 · 2021: 3 · 2020: 9 · 2019: 9 · 2018: 8 · 2017: 7 · 2016: 1
- FWCI
- 6.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Electrophoresis (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Forensic and Genetic Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- Y-chromosome SNPs, autosomal SNPs, sequencing noise, DNA mixture analysis, forensic genetics
- MeSH terms
- Denmark, Female, Humans, Male, Reproducibility of Results, Polymorphism, Single Nucleotide, White People, Forensic Genetics, High-Throughput Nucleotide Sequencing
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