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Massively parallel sequencing techniques for forensics: A review

机译:法医学的大规模平行测序技术:综述

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摘要

Abstract DNA sequencing, starting with Sanger's chain termination method in 1977 and evolving into the next generation sequencing (NGS) techniques of today that employ massively parallel sequencing (MPS), has become essential in application areas such as biotechnology, virology, and medical diagnostics. Reflected by the growing number of articles published over the last 2–3 years, these techniques have also gained attention in the forensic field. This review contains a brief description of first, second, and third generation sequencing techniques, and focuses on the recent developments in human DNA analysis applicable in the forensic field. Relevance to the forensic analysis is that besides generation of standard STR‐profiles, DNA repeats can also be sequenced to look for polymorphisms. Furthermore, additional SNPs can be sequenced to acquire information on ancestry, paternity or phenotype. The current MPS systems are also very helpful in cases where only a limited amount of DNA or highly degraded DNA has been secured from a crime scene. If enough autosomal DNA is not present, mitochondrial DNA can be sequenced for maternal lineage analysis. These developments clearly demonstrate that the use of NGS will grow into an indispensable tool for forensic science.
机译:摘要从1977年开始的Sanger链终止方法的DNA测序并发展到今天采用大规模平行测序(MPS)的下一代测序(NGS)技术,这在生物技术,病毒学和医学诊断等应用领域已经成为必不可少的。在过去2 - 3年内发表的越来越多的文章反映,这些技术也在法医领域得到了关注。本综述包含第一,第二代和第三代测序技术的简要描述,并专注于适用于法医领域的人体DNA分析的最新发展。与法医分析的相关性是除了产生标准的STR型谱之外,还可以测序DNA重复以寻找多态性。此外,可以对额外的SNP进行测序,以获取有关祖先,亲子符或表型的信息。当前的MPS系统在只有有限量的DNA或高度降解的DNA已从犯罪现场确保的情况下也非常有帮助。如果不存在足够的常血换DNA,则可以对线粒体DNA进行测序以进行母体谱系分析。这些发展清楚地表明,NGS的使用将成为法医学的不可或缺的工具。

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