ISO 17025 validation of a next‐generation sequencing assay for relationship testing
- 6 October 2016
- journal article
- research article
- Published by Wiley in Electrophoresis
- Vol. 37 (21) , 2822-2831
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.Keywords
This publication has 21 references indexed in Scilit:
- SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests?Transfusion Medicine and Hemotherapy, 2012
- Kinship Analysis with Diallelic SNPs – Experiences with the SNPforID Multiplex in an ISO17025 Accreditated LaboratoryTransfusion Medicine and Hemotherapy, 2012
- The SNPforID Assay as a Supplementary Method in Kinship and Trace AnalysisTransfusion Medicine and Hemotherapy, 2012
- A SNaPshot assay for genotyping 44 individual identification single nucleotide polymorphismsElectrophoresis, 2010
- Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and WindowsMolecular Ecology Resources, 2010
- Validation of a single nucleotide polymorphism (SNP) typing assay with 49 SNPs for forensic genetic testing in a laboratory accredited according to the ISO 17025 standardForensic Science International: Genetics, 2009
- SNPs for a universal individual identification panelHuman Genetics, 2009
- Performance of the SNPforID 52 SNP-plex assay in paternity testingForensic Science International: Genetics, 2008
- Forensically Relevant SNP ClassesBioTechniques, 2008
- A multiplex assay with 52 single nucleotide polymorphisms for human identificationElectrophoresis, 2006