METHOD OF DETECTING MUTATIONS ASSOCIATED WITH THROMBOSIS

The present invention provides a method for the simultaneous identification of two or more single base changes in a plurality of target nucleotide sequence s that are markers associated with cardiovascular diseases such as deep vein thrombosis and the like. Multiplex detection is accomplished using...

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Hauptverfasser: BLACK, MARGOT, KOBLER, DANIEL, BORTOLIN, SUSAN, JANECZKO, RICHARD A, FIELDHOUSE, DANIEL, MERANTE, FRANK, ZASTAWNY, ROMAN, MODI, HEMANSHU
Format: Patent
Sprache:eng ; fre
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Zusammenfassung:The present invention provides a method for the simultaneous identification of two or more single base changes in a plurality of target nucleotide sequence s that are markers associated with cardiovascular diseases such as deep vein thrombosis and the like. Multiplex detection is accomplished using multiplex ed tagged allele specific primer extension (ASPE) and hybridization of such extended primers to a probe, preferably an addressable anti-tagged support.< /SDOAB>