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Post-hoc comparisons were estimated using Bonferroni post-hoc test with correction for multiple comparisons.
The CD of comparisons were estimated using a sampling-based method that estimates empirical variances of true and predicted breeding values from a simulated n-sample.
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In addition, the fixation index (FST) values for each pairwise comparison were estimated using PoPoolation2 [ 110], by implementing a number of stringent criteria to define genomic sites for analysis across the entire genome.
P-values for comparisons of individual treatments were estimated using a Tukey honest significant difference test for multiple comparisons.
Pairwise comparisons and sequence characterizations were estimated using MEGA 4.0 [ 80].
The mean of each variable was calculated across 1,000 sets of 84 individuals drawn randomly (without replacement) from the 5,435 human individuals in the dataset, and these means were then used in all correlations and comparisons; among chimpanzees, quantities were estimated using all 84 individuals.
The alpha (biodiversity within samples) and beta (diversity comparison between samples) diversity values were estimated using tools implemented in the QIIME pipeline version 1.3.0.
As would be expected, respondent burden was substantially greater for those who completed all items in the scales, in comparison with those for whom scores were estimated using CAT.
These assignments were confirmed by comparison to prepared standards, and approximate concentrations were estimated using spectral deconvolution to estimate peak areas.
Differences between treatment groups were estimated using marginal means, with Sidak's adjustment for multiple comparisons.
Among-population genetic differentiation between the population pairs in each comparison mentioned above was estimated using the parameter (θRH).
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