使用Demixtify进行混合物检测

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY Forensic Science International-Genetics Pub Date : 2023-11-25 DOI:10.1016/j.fsigen.2023.102980
August E. Woerner , Benjamin Crysup , Jonathan L. King , Nicole M. Novroski , Michael D. Coble
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引用次数: 0

摘要

法医事实上的遗传标记是短串联重复序列(STRs)。有许多分析工具设计用于STRs,包括分析和评估DNA混合物的技术。相比之下,法医遗传谱系的新兴领域往往依赖于双等位基因单核苷酸多态性(SNPs)。为法医鉴定snp而设计的工具在一定程度上是缺乏的,尤其是DNA混合物。在本文中,我们介绍了Demixtify,一个程序,检测DNA混合物使用双等位基因snp。除杂是非常强大的;当覆盖率足够时,可以检测到高度不平衡的混合物(≤1:99,考虑到硅和体外混合物)。脱混也可以检测低覆盖率(~ 1x)样品中的混合物(当混合物相对平衡时)。除杂包括序列误差的经验估计,这是特定的标记分析,使其特别相关的法医界。正交技术也被用来表征体外混合物,以及被认为是单一来源的样品,这些方法的结果有助于验证所提出的技术。
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Mixture detection with Demixtify

The de facto genetic markers of forensics are short tandem repeats (STRs). There are many analytical tools designed to work with STRs, including techniques for analyzing and assessing DNA mixtures. In contrast, the nascent field of forensic genetic genealogy often relies on biallelic single nucleotide polymorphisms (SNPs). Tools designed for the forensic assessment of SNPs are somewhat lacking, especially for DNA mixtures. In this paper we introduce Demixtify, a program that detects DNA mixtures using biallelic SNPs. Demixtify is quite powerful; highly imbalanced mixtures can be detected (≤1:99, considering in silico and in vitro mixtures) when coverage is ample. Demixtify can also detect mixtures in low coverage (∼1×) samples (when the mixture is relatively balanced). Demixtify includes an empirical estimator of sequence error that is specific to the markers assayed, making it especially relevant to the forensic community. Orthogonal techniques are also developed to characterize in vitro mixtures, as well as samples thought to be single source, and the results of these approaches serve to validate the techniques presented.

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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.
期刊最新文献
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