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As described below, this method for evaluating experimental error was used in the mathematical modeling of log2AEI population distributions.
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Since, as we show below, an unbiased method for SNP effect assessment (e.g., GLM2) yields zero significant SNPs, any additional filtering step is superfluous, therefore we do not consider such filtering in the present work.
After completing one of the below methods for folding, use your thumb and forefinger to slip it into the pocket.
Below, we describe our method for detecting bright analyzable struts.
For this reason, this method is used for layers below the salt.
In the test cases for this method, described below, we used the well-known docking programs GOLD [9] and Glide [10].
Of course, we cannot exclude the possibility that smaller quantities of these siRNAs are below the threshold of detection for this method.
This method imputes a value for each datum below the method detection limit based on the method detection limit value, the percentage of observations below the method detection limit, and the mean and variance of the detected observations.
I predict the secondary structure of the coding sequences using the below methods and identify for each nucleotide whether it is paired with another nucleotide, or unpaired.
We initially placed SNARE core complex between model v- and t-membranes and calculated its interaction free energies with the two membranes at different lateral orientations (see below and Methods for details).
Different configurations are tested and we report only on the best below (see Methods for details).
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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