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In general, estimates of SDr and RSDr for both assays were within the acceptable range of a standard diagnostic test (Table 5).
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The divergence in the HBV DNA levels between both assays was within 0.5 log10 IU/mL and was found in only 10 samples.
The standard curve efficiency of both the ITS and IGS PCR assays were within the accepted range of 90%-11090%-110%
The limits of detection for these assays were within the range of other species-specific PCR assays for pine pathogens, in the picogram range of DNA detection (Duran et al. 2009; Ioos et al. 2010) and indicating a good level of PCR sensitivity.
98% of MARs in a 2.8 Mb region of chromosome 16 mapped by in vitro binding assays were within genic regions [50].
These experiments showed that peptide affinities determined in the two assays were within the margin of experimental error of each other (data not shown).
All enzymatic assays were within the minimal specifications.
Method validation focused on measuring precision and showed that 15 of the 17 assays were within acceptable limits.
The IL-2 sRα assay coefficients of variation were<6.1% (intra-assay) and<7.2% (inter-assay), and those for other assays were within a similar range.
Average amplification efficiency of the 17 gene assays in the Onco type DX Prostate Cancer Assay was 93%, and all gene assays were within ±6% of that value.
In this project, the calculated errors of the liquid enzymatic assays were within the minimal TE criterion of 13.3% for all five studied creatinine concentrations.
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CEO of Professional Science Editing for Scientists @ prosciediting.com