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In order to assess how well the use of a single fixed rate of evolution for the entire endoretroviral sequence would fit the MCMC results, we used four estimated rates of evolution and two intervals of rates for human ERVs from the literature, redoing the calculations for integration time with the methodology depicted in figure 1 (table 2).
The methodology, depicted in Fig. 3A, was based on a two-step positive/negative selection strategy.
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Research methodology depicted as a flow chart (Inventado et al. 2016).
A general overview of the methodology is depicted in Figure 1.
The methodology is depicted in Figure 1.
The general overview of the methodology is depicted in Figure 2. Two strategies for selecting the best phenotypic model were used in the first stage.
The bactericidal efficacy of our spray-on formulation (povidone-iodine aerosol foam), is compared to that of the traditional sponge-based application method using the methodology schematically depicted in Figure 1.
The methodology realistically depicts the various cracks common in an envelope in terms of shape, location, and quantity.
The flowchart of the whole methodology is depicted in Fig. 1.
We followed the similar methodology as depicted in Figure 3 to map the deepBase clusters (of size not more than 100 bp) onto the lncRNAs exonic regions.
The proposed methodology is depicted in Figure 4. To demonstrate the method, a series of simulation studies are performed.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com