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法医和古DNA研究中低拷贝数DNA样本的人类基因组特异性定量分析。

Specific quantification of human genomes from low copy number DNA samples in forensic and ancient DNA studies.

作者信息

Alonso Antonio, Martin Pablo, Albarrán Cristina, García Pilar, Primorac Dragan, García Oscar, Fernández de Simón Lourdes, García-Hirschfeld Julia, Sancho Manuel, Fernández-Piqueras Jose

机构信息

Instituto Nacional de Toxicología, Servicio de Biología, Luis Cabrera 9, 28002 Madrid, Spain.

出版信息

Croat Med J. 2003 Jun;44(3):273-80.

Abstract

We reviewed the current methodologies used for human DNA quantitation in forensic and ancient DNA studies, including sensitive hybridization methods based on the detection of nuclear alpha-satellite repetitive DNA regions or more recently developed fluorogenic real-time polymerase chain reaction (PCR) designs for the detection of both nuclear and mitochondrial DNA regions. Special emphasis has been put on the applicability of recently described different real-time PCR designs targeting different fragments of the HV1 mtDNA control region, and a segment of the X-Y homologous amelogenin gene. The importance of these quantitative assays is to ensure the consistency of low copy number DNA typing (STR profiling and mtDNA sequencing).

摘要

我们回顾了法医和古DNA研究中用于人类DNA定量的当前方法,包括基于检测核α卫星重复DNA区域的灵敏杂交方法,以及最近开发的用于检测核DNA和线粒体DNA区域的荧光实时聚合酶链反应(PCR)设计。特别强调了最近描述的针对HV1线粒体DNA控制区域不同片段以及X-Y同源牙釉蛋白基因片段的不同实时PCR设计的适用性。这些定量分析的重要性在于确保低拷贝数DNA分型(STR分型和线粒体DNA测序)的一致性。

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