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The applied velocity steps are indicated in micrometre per second (μm/s), with the location of a change in velocity indicated using dashed lines connecting the same velocity step in different experiments.
Individual on-chip compartments referred to in different steps are indicated in Figure 2 with a few distinctive chip features shown in greater detail in Figure 3.
Low probability event combinations falling into the range occupied by unitary steps are indicated under the velocity curve in panels A and C of Figure 4 in the smaller font.
Five key steps are indicated with red numbers: 1 TFEα and TFEβ WH domains are related to bacterial MarR-type WH domains indicating their early evolutionary origin (Aravind et al., 2005 ; Blombach et al., 2009 ).
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As an example, an approx. 0.35-nm and an approx. 1.1-nm high step are indicated in Figure 1c.
Note –Features that were removed in the feature selection step are indicated by ns.
Ratio of the results by software to favorite results in each step is indicated by R, if R be closer to 1 it means that obtained results by software is closer to observed result.
The number of generations passing between each step is indicated, based on a change of only 0.005% in some parameter (length, width, or protein density) per generation with changes resulting in an improved calculated image formation retained each time.
The direction of each updating step was indicated by a centrally presented colored arrow; the arrow's color determined which circle the update was to be applied to.
The end of this perfusion step is indicated by a light-red color of the out-flowing perfusion solution I. Note: To avoid a loss of perfusion pressure, any vessel leakage should be immediately stopped by using additional tissue glue.
The edited alignments can be found in the additional material (additional file 4: dmt.aln.tgz), and the new number of sequences after this step is indicated in parentheses in Table 1.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com