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Selected data were analyzed by chi-squared tests and Fischer's exact probability tests (α = 0.05).
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A large repository of diverse specimens from HIV-positive patients was established, multiple assays were run on 2500 selected specimens, and data were analyzed to estimate assay characteristics relevant for incidence surveillance.
Eight genes selected from the array data were analyzed by quantitative real-time PCR (qPCR) in seven patients and seven controls (these subjects were selected based on quantity of RNA remaining after microarrays).
The levels of gene expression of 18 candidate genes selected from the 454 data were analyzed in a non-treated (Control) and in the two groups (R1 and R2) that survived to dichlorvos treatment.
After excluding incorrect results and individuals not meeting the inclusion criteria, a selection process without a repetition option using Statistica software was performed to randomly select 130 patients whose data were analyzed.
The L25 56) orthogonal array was selected for the experiment and data were analyzed by means of the analysis of range (ANORA) and the analysis of variance (ANOVA).
Associations between accumulation of host-derived SMCs and predictors of cellular accumulation selected from demographical, biochemical/functional, and immunohistochemical data were analyzed by best-subset logistic regression.
For identification of differentially expressed microRNAs data were analyzed by cluster analysis and selected statistical methods.
Other data were analyzed and compared by using ANOVA and selected post hoc tests.
Data were analyzed descriptively.
Obtained data were analyzed.
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