DNA mixture analyses of autosomal single nucleotide polymorphisms for individual identification using droplet digital polymerase-chain reaction and massively parallel sequencing in combination with EuroFormix
Journal
Australian Journal of Forensic Sciences
Journal Volume
57
Journal Issue
2
Start Page
170
End Page
183
Date Issued
2025
Author(s)
Abstract
Droplet digital polymerase-chain reaction (ddPCR) and massively parallel sequencing (MPS) can be used to detect an extremely low proportion of non-overlapping single nucleotide polymorphisms (SNPs) of a minor contributor in a DNA mixture. Both semi-continuous and continuous probabilistic likelihood ratio (LR) models can be used to interpret the DNA profiles of mixtures. We analysed 28 identity-informative SNPs in 20 DNA mixtures with various minor to major ratios (1:29, to 1:99) by using our customized ddPCR panel and two MPS panels. The minor contributors of the DNA mixtures were correctly inferred using both semi-continuous and continuous LR models of EuroForMix based on the data of our customized ddPCR and one MPS panel. The accuracy rate of minor contributor assignment was 95% and 90% using semi-continuous and continuous LR models, respectively, using the data of the other MPS panel with lower coverage reads. In conclusion, the quantitative genotype data of SNPs generated using ddPCR can be used for the minor contributor inference for DNA mixtures. The performance of a continuous LR model in minor contributor identification in DNA mixtures may not be superior to that of a semi-continuous LR model when the coverage reads of the MPS panel is insufficient.
Subjects
continuous likelihood ratio | Droplet digital PCR | massively parallel sequencing | semi-continuous likelihood ratio | single nucleotide polymorphism
SDGs
Type
journal article