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US07879543B2 Method of detecting mutations associated with thrombosis 有权
检测与血栓形成相关的突变的方法

Method of detecting mutations associated with thrombosis
Abstract:
The present invention provides a method for the simultaneous identification of two or more single base changes in a plurality of target nucleotide sequences that are markers associated with cardiovascular diseases such as deep vein thrombosis and the like. Multiplex detection is accomplished using multiplexed tagged allele specific primer extension (ASPE) and hybridization of such extended primers to a probe, preferably an addressable anti-tagged support.
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