用于人类识别的射枪 DNA 测序:考虑误差的动态 SNP 选择和似然比计算

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY
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引用次数: 0

摘要

枪式测序是一种 DNA 分析方法,可确定样本中每个 DNA 片段的核苷酸序列,与广泛应用于法医遗传学的基于 PCR 的基因分型方法不同,枪式测序针对的是预定义的短串联重复序列 (STR) 或预定义的单核苷酸多态性 (SNP)。枪式DNA测序尤其适用于高度降解的低质量DNA样本,如古代样本或来自犯罪现场的样本。在此,我们利用散弹枪测序数据建立了一个人类识别统计模型,并开发了以似然比 (LR) 计算证据权重的公式。该模型使用一组动态的二元 SNP 位点,并以概率的方式考虑了霰弹枪测序的错误率。据我们所知,该方法是第一种能做到这一点的方法。口腔拭子(高质量样本)和头发样本(低质量样本)的重复猎枪测序结果被排列在基因型-调用混淆矩阵中,通过最大似然法和贝叶斯推断法估计调用错误概率。不同的基因型质量过滤器可用于考虑基因分型误差。错误概率为零时,常用 LR 公式计算证据权重。错误概率高于零会降低匹配基因型的 LR 贡献,而在痕量基因型与相关人员基因型不匹配的情况下,LR 会增加。在后一种情况下,LR 从零(发生在错误概率为零时)增加到低正值,这就考虑到了不匹配可能是由于基因分型错误造成的。我们开发了一个开源 R 软件包 wgsLR,用于实现该方法,包括估计调用错误概率和计算 LR 值。R 软件包包括本文使用的所有公式以及生成公式的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Shotgun DNA sequencing for human identification: Dynamic SNP selection and likelihood ratio calculations accounting for errors

Shotgun sequencing is a DNA analysis method that potentially determines the nucleotide sequence of every DNA fragment in a sample, unlike PCR-based genotyping methods that is widely used in forensic genetics and targets predefined short tandem repeats (STRs) or predefined single nucleotide polymorphisms (SNPs). Shotgun DNA sequencing is particularly useful for highly degraded low-quality DNA samples, such as ancient samples or those from crime scenes. Here, we developed a statistical model for human identification using shotgun sequencing data and developed formulas for calculating the evidential weight as a likelihood ratio (LR). The model uses a dynamic set of binary SNP loci and takes the error rate from shotgun sequencing into consideration in a probabilistic manner. To our knowledge, the method is the first to make this possible. Results from replicated shotgun sequencing of buccal swabs (high-quality samples) and hair samples (low-quality samples) were arranged in a genotype-call confusion matrix to estimate the calling error probability by maximum likelihood and Bayesian inference. Different genotype quality filters may be applied to account for genotyping errors. An error probability of zero resulted in the commonly used LR formula for the weight of evidence. Error probabilities above zero reduced the LR contribution of matching genotypes and increased the LR in the case of a mismatch between the genotypes of the trace and the person of interest. In the latter scenario, the LR increased from zero (occurring when the error probability was zero) to low positive values, which allow for the possibility that the mismatch may be due to genotyping errors. We developed an open-source R package, wgsLR, which implements the method, including estimation of the calling error probability and calculation of LR values. The R package includes all formulas used in this paper and the functionalities to generate the formulas.

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来源期刊
CiteScore
7.50
自引率
32.30%
发文量
132
审稿时长
11.3 weeks
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.
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