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QPCR data of the genes of interest were normalized based on the expression of the reference genes using the normalization factor from geNORM.
The recorded working heart rates were normalized based on the maximum heart rate obtained during maximum aerobic power measurement.
The TPD profiles were normalized based on the N2 signal intensity.
A tally of overlaps (migrations) was determined between each sampled location and counts were normalized based on metagenome sizes.
Secant stiffnesses of test specimens were normalized based on the stiffness at first cycle of 0.15% drift ratio and shown in Fig. 23.
Singletons, non-bacterial OTUs were removed, and the OTU abundance levels were normalized based on the sample with the least number of sequences.
In this study, individual samples were normalized based on the volume ratio of the original whole blood samples to the resulting products (Table 1).
Figure 8 shows the residuals between the responses observed and predicted from the final model, which were normalized based on the relative errors (delta Z/left| Z right|) after applying the error floors.
Sample volumes were normalized based on the total protein content determined by the Bradford assay.
cGMP levels were normalized based on the amount of protein present.
Data were normalized based on the control on the TLDA card and analyzed.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com