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The heteroplasmy detection threshold was set to 0.2%; the sensitivity and specificity of detected heteroplasmies were determined from 12 samples (one sample was discarded after quality filters) whose levels of heteroplasmy were measured using 3 different PCR products.
Total biomass, ear number, sample grain weight and kernel weight should be determined from this sample.
Comparisons between sets of angular distributions were made using the 2-sided Kolmogorov Smirnov (K S) test, which determines whether 2 sample sets have been drawn from the same distribution (Kolmogorov 1933; Smirnov 1939; Massey 1951).
Melatonin levels were determined from plasma samples that were collected from each groups.
For each experiment, average dead/live ratios were determined from triplicated samples.
The similar ratios of difference were determined for blocked M13KO7 sample sets at a cut off of 1-fold.
Serum MT levels were determined from arterial blood samples.
The borders in Fig. 5A are determined from the average of six different sets of Nissl-stained samples.
A calibration plot was created of the actual temperature inside the CD sample cell (determined from a thermocouple reading) versus the set temperature.
Background levels ascribed to each fraction were determined from a specific set of samples collected from relatively pristine areas in the upper Seine basin and validated on prehistoric samples.
The relative abundance of the targeted mRNAs from several samples was determined from a standard curve that was constructed from a set of DNA dilutions from each one of the transcripts to be analyzed.
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CEO of Professional Science Editing for Scientists @ prosciediting.com