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A MEMS-based approach to single nucleotide polymorphism genotyping

机译:基于MEMS的单核苷酸多态性基因分型方法

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摘要

Genotyping of single nucleotide polymorphisms (SNPs) allows diagnosis of human genetic disorders associated with single base mutations. Conventional SNP genotyping methods are capable of providing either accurate or high-throughput detection, but are still labor-, time-, and resource-intensive. Microfluidics has been applied to SNP detection to provide fast, low-cost, and automated alternatives, although these applications are still limited by either accuracy or throughput issues. To address this challenge, we present a MEMS-based SNP genotyping approach that uses solid-phase-based reactions in a single microchamber on a temperature control chip. Polymerase chain reaction (PCR), allele specific single base extension (SBE), and desalting on microbeads are performed in the microchamber, which is coupled with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) to analyze the SBE product. Experimental results from genotyping of the SNP on exon 1 of the HBB gene, which causes sickle cell anemia, demonstrate the potential of the device for rapid, accurate, multiplexed and high-throughput detection of SNPs.
机译:单核苷酸多态性(SNP)的基因分型可以诊断与单碱基突变相关的人类遗传疾病。常规的SNP基因分型方法能够提供准确的或高通量的检测,但是仍然需要大量的劳动,时间和资源。微流体技术已应用于SNP检测,以提供快速,低成本和自动化的替代方法,尽管这些应用仍然受到准确性或通量问题的限制。为了解决这一挑战,我们提出了一种基于MEMS的SNP基因分型方法,该方法在温度控制芯片上的单个微腔中使用基于固相的反应。在微腔室中进行聚合酶链反应(PCR),等位基因特异性单碱基延伸(SBE)和微珠脱盐,并与基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)结合使用分析SBE产品。对导致镰状细胞性贫血的HBB基因外显子1进行SNP基因分型的实验结果表明,该设备具有快速,准确,多重和高通量检测SNP的潜力。

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