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The activation/maturation status of DCs was evaluated by analyses of CD86 and CD83 expression.
Group differences were evaluated by analyses of variance with the between factor GROUP and the within factors HEMISPHERE (left/right), GRADIENT (central/posterior) and ROW (dorsal/ventral) for the contrast scores for 8 selected areas covering temporal regions in both hemisphere, and the unsupervised clustering scores.
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The accuracy of the proposed method was evaluated by analysing of SRM Apple Leaves 1515 certified reference material.
The precision and accuracy of the UHPLC method were evaluated by analysing blank samples of urine spiked with high, medium, and low concentrations of the flavonoids and isoflavones.
Specificity of the final choice of antibody for XIAP was evaluated by analysing a panel of cell lines including clone X-G4.
Therefore, the dynamics of the free expansion process was evaluated by analysing the convergence of four parameters: 1. Mean nodal distance metric is the average distance from the vertices of the current expanding stent to their counterparts in the load-free device.
The infection process of pea roots with A. euteiches and P. pisi was evaluated by analysing gene expression of selected defence marker genes such as ACO (1-aminocyclopropane-1-carboxylate oxidase), Pi49 (PR10-like), ABA17 (abscisic acid responsive gene) and chit4 (chitinase 4), using reverse transcription quantitative PCR (RT-qPCR).
Repeatability was evaluated by analysing 3 replicates of each sample.
Different pre-processing methods were evaluated by analysing the variance of the resulting gene expression intensities via various statistical measures.
The completeness of the N. furzeri proteins represented in the transcript catalogue was evaluated by analysing the proportion of coding sequence (CDS).
This is evaluated by analysing the process of answering questionnaire items, identifying how and when an item does not achieve its objective [ 24, 33].
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CEO of Professional Science Editing for Scientists @ prosciediting.com