Elsevier, Forensic Science International: Genetics Supplement Series, 1(1), p. 19-21
DOI: 10.1016/j.fsigss.2007.10.111
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High levels of non-authentic sequence data can be generated by traditional PCR-based methodologies when DNA is damaged, template numbers are small and/or the target amplification size too large. We therefore present an alternate methodology based on single primer extension (SPEX) amplification; that places no pre-defined size constraints on amplification and interacts with only one of the DNA strands at the target locus.