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多色探针熔解曲线分析技术在代谢酶相关基因突变检测中的研究和应用

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ed that 0sampleshad mutations omsMe therange of our syStem while 8samples had fullyconcordant result.The specificity of our method was thus 00%pared with sequencing. Inchapter 3,we firstgave abriefintroduction ofpharmacogenomics by usillg warfarin and clopidogrel asexamples.We then described the establishment of atwo -reaction,four—color MMCA assay thatcould detect 8com.rnon SNPs useful for administration ofwarfarin and clopidogrel.As low as50pg/reaction genomic DNA Can bed嗽ted reliably.This MMCA assay was thenused toanalyze 27samples andthefi-equencies of8SNPs were calculated.Weconcluded thatthisnew method 3 Abswaa could provide arapid,accurate,sensitive toolforwarfarin and clopidogrel interms of pharmacogenomics Key words:mukicolor meking curve analysis;G6PD deficiency;pharmacogenomics 4

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