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There was large variation across studies in all correlations as indicated by the Q statistics.
Recombination does not significantly affect any phylogenetic parameter (P > 0.5 in all correlations; results not shown).
In all correlations between EEG data and posterror adjustment, we used Spearman's correlations.
In all correlations shown throughout this paper, a threshold of 1.5 Å is employed to emphasize those residues that are actually moving significantly during the simulation.
Single-cell analyses involving one dichotomous and one continuous variable (also tested for outliers) were Wilcoxon rank-sum tests in all correlations, except for the ones quantifying modulation in the ISI relative to baseline and the difference in CR amplitude between MLI mutants and wild-types across sessions, which was tested with a Wilcoxon matched-pair signed-rank test.
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.
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The P value in all these correlations were <0.05.
Establishing causation is a difficulty in this work, as in all correlation network analyses.
The same leg of injured and uninjured players was thus compared in all correlation analysis.
This assures that a similar number of ties is maintained in all correlation analyses.
In all correlation analyses pair wise Pearson correlations between signatures were computed independently for the human and dog datasets, after removing the normal samples.
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