清脆的
核酸检测
核酸
生物
分子诊断学
计算生物学
病菌
基因组编辑
纳米技术
基因
计算机科学
生物信息学
遗传学
材料科学
作者
Jian Zhang,Hailong Lv,Linxian Li,Minjie Chen,Dayong Gu,Jin Wang,Yong Xu
标识
DOI:10.3389/fmicb.2021.751408
摘要
Molecular diagnostic (MDx) methods directly detect target nucleic acid sequences and are therefore an important approach for precise diagnosis of pathogen infection. In comparison with traditional MDx techniques such as PCR, the recently developed CRISPR-based diagnostic technologies, which employ the single-stranded nucleic acid trans-cleavage activities of either Cas12 or Cas13, show merits in both sensitivity and specificity and therefore have great potential in both pathogen detection and beyond. With more and more efforts in improving both the CRISPR trans-cleavage efficiencies and the signal detection sensitivities, CRISPR-based direct detection of target nucleic acids without preamplification can be a possibility. Here in this mini-review, we summarize recent research progresses of amplification-free CRISPR-Dx systems and explore the potential changes they will lead to pathogen diagnosis. In addition, discussion of the challenges for both detection sensitivity and cost of the amplification-free systems will also be covered.
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