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Pyrosequencing of clinically relevant polymorphisms.

Sharon Marsh·Cristi R King·Adam A Garsa·Howard L McLeod
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Abstract

The data generated from the Human Genome Project has led to an explosion of technology for low-, medium-, and high-throughput genotyping methods. Pyrosequencing is a genotyping assay based on sequencing by synthesis. Short runs of sequence around each polymorphism are generated, allowing for internal controls for each sample. Pyrosequencing can also be used to identify tri-allelic, indel, and short-repeat polymorphisms, as well as determining allele percentages for methylation or pooled sample assessment. Assays details for Pyrosequencing of clinically relevant polymorphisms are described in this chapter.

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Adenosine TriphosphateAllelesCytochrome P-450 CYP3ACytochrome P-450 Enzyme SystemGenetic Predisposition to DiseaseGenotypeHumansATP-Binding Cassette, Sub-Family C ProteinsPolymerase Chain ReactionPolymorphism, Single NucleotideSequence Analysis, DNAJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, U.S. Gov't, P.H.S.

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Sharon Marsh, Cristi R King, Adam A Garsa, Howard L McLeod. 2005. Pyrosequencing of clinically relevant polymorphisms.. https://doi.org/10.1385/1-59259-957-5%3A097

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