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).
| Original language | English (US) |
|---|---|
| Pages (from-to) | 273-280 |
| Number of pages | 8 |
| Journal | Croatian Medical Journal |
| Volume | 44 |
| Issue number | 3 |
| State | Published - Jun 2003 |
All Science Journal Classification (ASJC) codes
- General Medicine
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