http://hdl.handle.net/2440/74227 2013-06-19T01:32:46Z 2013-06-19T01:32:46Z Brotherton, Paul Michael Sanchez, Juan J. Cooper, Alan Endicott, Phillip http://hdl.handle.net/2440/59941 2012-11-13T23:34:13Z 2009-12-31T13:30:00Z

Title: Preferential access to genetic information from endogenous hominin ancient DNA and accurate quantitative SNP-typing via SPEX Author: Brotherton, Paul Michael; Sanchez, Juan J.; Cooper, Alan; Endicott, Phillip Abstract: The analysis of targeted genetic loci from ancient, forensic and clinical samples is usually built upon polymerase chain reaction (PCR)-generated sequence data. However, many studies have shown that PCR amplification from poor-quality DNA templates can create sequence artefacts at significant levels. With hominin (human and other hominid) samples, the pervasive presence of highly PCR-amplifiable human DNA contaminants in the vast majority of samples can lead to the creation of recombinant hybrids and other non-authentic artefacts. The resulting PCR-generated sequences can then be difficult, if not impossible, to authenticate. In contrast, single primer extension (SPEX)-based approaches can genotype single nucleotide polymorphisms from ancient fragments of DNA as accurately as modern DNA. A single SPEX-type assay can amplify just one of the duplex DNA strands at target loci and generate a multi-fold depth-of-coverage, with non-authentic recombinant hybrids reduced to undetectable levels. Crucially, SPEX-type approaches can preferentially access genetic information from damaged and degraded endogenous ancient DNA templates over modern human DNA contaminants. The development of SPEX-type assays offers the potential for highly accurate, quantitative genotyping from ancient hominin samples.

2009-12-31T13:30:00Z