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

被引:0
|
作者
Alonso, A
Martín, P
Albarrán, C
García, P
Primorac, D
García, O
de Simón, LF
García-Hirschfeld, J
Sancho, M
Fernández-Piqueras, J
机构
[1] Inst Nacl Toxicol, Serv Biol, Madrid 28002, Spain
[2] Split Univ Hosp, Lab Clin & Forens Genet, Split, Croatia
[3] Area Lab Ertzaintza, Bilbao, Spain
[4] Univ Autonoma Madrid, Lab Genet Mol Humana, Madrid, Spain
关键词
DNA; DNA fingerprinting; DNA mitochondrial; evolution; forensic medicine; polymerase chain reaction; tandem repeat sequences;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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).
引用
收藏
页码:273 / 280
页数:8
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