Ye‑Lim Kwon , Jiwon Kim , Su Min Joo , Kyoung‑Jin Shin
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引用次数: 0
Abstract
With the advent of phase-known sequencing enabled by massively parallel sequencing (MPS), research on microhaplotypes (microhaps), multi-single nucleotide polymorphisms within short DNA fragments, has advanced significantly in forensic genetics. However, MPS data inherently contains PCR and sequencing errors, presenting challenges in distinguishing minor contributor alleles from background noise in DNA mixture analysis. Divisive Amplicon Denoising Algorithm 2 (DADA2) has been widely used in microbial research for inferring amplicon sequence variants (ASVs) through computational error correction. However, its potential applicability to forensic identity testing has not been fully explored. In this study, we redesigned an in-house MPS panel targeting 24 multipurpose microhaps and established a pipeline employing DADA2’s ASV inference algorithm to denoise microhap MPS data. Denoising performance was evaluated using 1 ng of DNA from 50 single-source samples. The average not suppressed noise level decreased from 1.2 % to 0.1 % after denoising, achieving a genotype concordance rate of 99.5 % with undenoised data. However, DADA2 had difficulty in distinguishing heterozygous alleles differing only by single indel. In two-person DNA mixture analysis, DADA2-denoising pipeline reduced the number of noise haplotypes by 10-fold across various ratios (1:10, 1:20, 1:50, and 1:100) using 1 ng of total DNA. Even at a 1:100 ratio with 10 pg of minor DNA, noise was detected in only two or fewer markers among the 24 microhaps. These findings highlight the potential of computational error correction for enhancing the accuracy of detecting minor alleles and estimating the number of contributors in forensic analyses.
期刊介绍:
Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts.
The scope of the journal includes:
Forensic applications of human polymorphism.
Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies.
Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms.
Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications.
Non-human DNA polymorphisms for crime scene investigation.
Population genetics of human polymorphisms of forensic interest.
Population data, especially from DNA polymorphisms of interest for the solution of forensic problems.
DNA typing methodologies and strategies.
Biostatistical methods in forensic genetics.
Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches.
Standards in forensic genetics.
Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards.
Quality control.
Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies.
Criminal DNA databases.
Technical, legal and statistical issues.
General ethical and legal issues related to forensic genetics.