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Our next analysis is by simulation of the pathway under inhibition of multiple reactions.
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The next analysis was evaluation of ability to inhibition lipid peroxidation (LPO).
The next analysis was a hypothesis-free screen based on the genome-wide extent of CUB.
Hence, our next analysis was to determine if sequence artefacts were also present in our cohort of recently fixed samples.
The next analysis was to establish the probability of finding a particular surface type carious for each DMF score.
Then next analysis was performed when they reached the steady learning curve with achieving over 90% SCI at next 250 300 cases respectively.
Our next analysis was aimed at determining which genes were uniquely detected in each cell type and could therefore serve as an expression signature for that cell type.
The next analysis was to determine whether correct or incorrect choices, and treatment group were associated with mean log latency to choose (choice latency).
Each DNA sample for next-analysis was the mixture of three independent DNA extractions from one compost sample.
Most DNA-based diagnostics nowadays involve Sanger sequencing, which clinicians are comfortable with, and we need to really establish that what we are getting from next-generation analysis is in many ways better, but at least equivalent.
As a next step this analysis is extended to the case with extinction (zeta >) 0. In this case the analysis requires slightly more work; here for convenience the t is left out of the expressions.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com