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Primers for Dengue Virus Strains Based on Their Sequence Variability

机译:基于其序列变异性的登革热病毒菌株引物

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Since DENV-1, 2, 3, and 4 determine the strains for dengue virus, their gene sequence can be used as marker for diagnosis, amplifying and genotyping subtypes in molecular screening reaction which includes RT-PCR, real-time RT-PCR, nucleic acid sequence-based amplification, microsphere-based duplexed immunoassay, and DNA microarrays. There are many gene based PCR diagnostic kits available for screening and quantifying dengue virus, which one to choose? Decisions on choosing the diagnostic kit are debatable, mainly because of sequence variation of endemic dengue virus, which emphasizes us to use region specific primer diagnostic kits for isolating dengue of the prevailing country. But if diagnoistic industry focuses on the homologous regions obtained after aligning sequences, each representing the country of origin, we can design primers which can be used to detect dengue strains from any country of origin. Gene based diagnostics kits should have primers that should be covered for all entries present in the NCBI database with 100% total coverage similarity and specifically only to which they were designed for.
机译:由于DENV-1、2、3和4决定了登革热病毒的菌株,因此它们的基因序列可用作分子筛选反应的诊断,扩增和基因分型的标记,包括RT-PCR,实时RT-PCR,基于核酸序列的扩增,基于微球的双重免疫测定和DNA微阵列。有许多基于基因的PCR诊断试剂盒可用于筛选和定量登革热病毒,该选择哪一种?选择诊断试剂盒的决定值得商de,主要是因为地方性登革热病毒的序列变异,这突显了我们使用区域特异性引物诊断试剂盒来分离流行国家的登革热。但是,如果诊断行业着眼于比对序列后获得的同源区域,每个区域都代表起源国,我们可以设计引物,用于检测来自任何起源国的登革热菌株。基于基因的诊断试剂盒应具有所有NCBI数据库中所有条目均应覆盖的引物,且总覆盖率100%相似,并且仅针对其设计用途。

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