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EDTA tubes were centrifuged and a cellular layer with the intention of later DNA analysis was removed.
The stimulus-driven activity was removed through 2 steps (Supplementary Fig. 2): First, the stimulus-driven activation as modeled in the GLM analysis was removed, resulting in a residual time series response for each participant.
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Another key to the sensitivity of our analysis was removing samples that showed subtle technical defects.
Variables that did not reach statistical significance at the p ≤ 0.05 level in the regression analysis were removed, but were subsequently retained if their removal changed the magnitude of the main effect by more than 10%.
The arrows show the locations where samples for cross-section analysis were removed (a).
Even if our own counter analysis is removed from the calculation, showing numerous kidney dysfunctions [2], around 32% of disturbances are still noticed in kidneys.
The sign ambiguities, which always occur in the process of single closed fringe pattern analysis, are removed through the discontinuities of the angle in the 2-D wavelet ridge.
The arrows show the approximate locations where microsamples for cross-section analysis were removed from (a); Pb (b), Zn (c), Co (d), and Br (e) distribution maps acquired by XRF imaging.
Samples for cytokine analysis were removed before adding the bacteria to the blood and after 90 min of incubation.
Samples for transcriptome analysis were removed immediately after mixing the bacteria with human blood, and after 30 and 90 min of incubation.
Compounds that failed this analysis were removed, leaving 115 compounds.
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CEO of Professional Science Editing for Scientists @ prosciediting.com