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The samples were considered genotoxic if the induction factor exceeded 1.5 (exposed bacteria versus negative control) measured at 405 nm.
The samples were considered to be soluble if a single-phase, clear, gel-free solution was observed.
The integrity of the samples were considered to be maintained if -%nominal is within ± 15%of nominal values and %CVs ≤ 15%at both diluted levels.
According to the Guiding Principles of Hemolysis Test [H]GPT4-1, the samples were considered as hemolytic if the hemolytic percentage was above 5%.
The samples were considered stable in plasma at each concentration if the deviation from the mean calculated concentration of stability quality control samples was within ±15%.
Only those elements that were above the limit of detection of the ICP-MS in all or most (>90 %) of the samples were considered suitable for statistical analysis.
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The culture medium without the extracts of the samples was considered as the control.
A subclass that contained at least 10% of the samples was considered as a possible candidate subclass.
In qualitative detection, the samples are considered positive if DNA is detected (presence vs. absence).
The predominant allele (>50% of the samples) was considered the wild-type allele, and was used as the reference sequence.
Above this threshold value, the fluorescence of the samples is considered to be above the background contribution [ 5].
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CEO of Professional Science Editing for Scientists @ prosciediting.com