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The assay based on reverse hybridization principle simultaneously detects 13 different mutations affecting 6 independent codons, including the most prevalent mutations at positions 531 and 526.
Molecular line probe assays (LPA) for rapid detection of MDR-TB, which are based on reverse hybridization technology have been endorsed by WHO in 2009 [ 9].
In this case, in particular in presence of cervico-facial localization, the differentiation of tubercular from non-tubercular etiology is crucial and may be confidently achieved by resorting to methods based on reverse hybridization, which are commercially available.
The LiPA 2.0 assay is a commercially available HCV genotyping assay that is based on reverse hybridization of the 5′-nontranslated region (NTR) and core regions of the HCV genome to immobilized oligonucleotide probes (29).
This assay is based on reverse hybridization between rpoB amplicons and membrane-bound capture probes (1 specific for MTBC, 5 overlapping wild-type probes spanning the rpoB target region, and 4 of the most common mutations).
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False positive identifications were based on reverse database analysis.
Hepcell is based on reverse passive haemagglutination technology.
REBA MTB-Rifa® (YD Diagnostics, Yongin-si, South Korea) [ 18] is a commercially available LPA based on the reverse hybridization principle that specific oligonucleotide probes are immobilized on a membrane and hybridized under strictly controlled conditions with the biotin-labeled PCR product.
The test is based on the reverse hybridization principle.
DNA strip technology (line probe assays) based on the reverse hybridization of PCR products to their complementary probes has been used for the simultaneous detection and identification of mycobacteria.
HCV genotypes/subtypes were determined with a commercially available assay based on the reverse-hybridization principle.
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based on reverse ray-tracing
based on reverse micro-emulsion
based on reverse strength
based on reverse auction
based on reverse piloting
based on reverse osmosis
based on reverse order
based on reverse causality
based on reverse analysis
based on reverse vaccinology
based on reverse transcription PCR
based on reverse flow
based on reverse lookup
based on reverse database
based on reverse transcriptase
based on reverse passive
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