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Separating human DNA mixtures using denaturing high-performance liquid chromatography.

Phillip B Danielson·Richard Kristinsson·Robert J Shelton·Greggory S Laberge
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Abstract

DNA mixtures represent challenging samples that are rarely amenable to direct DNA sequence analysis and many of the strategies available to separate mixtures are both labor and time intensive. Denaturing high-performance liquid chromatography is an accurate and rapid approach for the detection and scoring of mutations. It can also be used to separate DNA mixtures. The technique relies on the chromatographic separation of crosshybridization products to isolate the individual components of a mixture. By eliminating secondary amplification and excessive manipulation prior to sequencing, denaturing high-performance liquid chromatography can streamline the analysis of conditions ranging from somatic mosaicism, microchimerism and mitochondrial heteroplasmy to evidentiary material containing mixtures of DNA encountered in forensic investigations.

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ChimerismChromatography, High Pressure LiquidDNADNA, MitochondrialGenetic MarkersHumansMosaicismSequence Analysis, DNAJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.Review

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Phillip B Danielson, Richard Kristinsson, Robert J Shelton, Greggory S Laberge. 2005. Separating human DNA mixtures using denaturing high-performance liquid chromatography.. https://doi.org/10.1586/14737159.5.1.53

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