2022
DOI: 10.1016/j.talanta.2021.122974
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A novel microfluidic RNA chip for direct, single-nucleotide specific, rapid and partially-degraded RNA detection

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Cited by 4 publications
(2 citation statements)
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“…Combined with reverse transcription recombinase-assisted amplification (RT-RAA), it overcomes the limitations of the NoV detection technology and effectively reduces time, cost and dependence on instruments. In contrast to methods using reverse transcription, Zhang et al [66] reported a new microfluidic RNA microarray (MIRC, a prototype of microchips) strategy based on the genomic replication of DNA polymerase-extended RNA primers on DNA templates with dNTP [67,68], which allowed the direct detection of RNAs without the need for reverse transcription, thus overcoming the tedious reverse transcription process. The method is characterized by rapid detection (within 20 min), high sensitivity, automation and high throughput [69,70].…”
Section: Microchip-based Rna Biosensorsmentioning
confidence: 99%
“…Combined with reverse transcription recombinase-assisted amplification (RT-RAA), it overcomes the limitations of the NoV detection technology and effectively reduces time, cost and dependence on instruments. In contrast to methods using reverse transcription, Zhang et al [66] reported a new microfluidic RNA microarray (MIRC, a prototype of microchips) strategy based on the genomic replication of DNA polymerase-extended RNA primers on DNA templates with dNTP [67,68], which allowed the direct detection of RNAs without the need for reverse transcription, thus overcoming the tedious reverse transcription process. The method is characterized by rapid detection (within 20 min), high sensitivity, automation and high throughput [69,70].…”
Section: Microchip-based Rna Biosensorsmentioning
confidence: 99%
“…Since many life-threatening infectious diseases have similar signs and symptoms, such as cold or u-like syndromes, accurate detection of the pathogens is therefore essential to provide correct treatment regimes. RNA has been recognized as a major biomarker of living pathogens, especially life-threatening RNA viruses like severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) and inuenza virus, 1,2 and thus reliable and accurate RNA detection methods are greatly required for pathogen identication and epidemic control. 3 Nucleic acid amplication tests (NAATs) are the most used RNA detection approaches at present due to their excellent sensitivity and high efficiency, among which quantitative reverse transcription polymerase chain reaction (qRT-PCR) is the most well known and has been considered the gold standard for SARS-CoV-2 detection.…”
Section: Introductionmentioning
confidence: 99%