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Participation rates and participant characteristics were assessed using all available data on the entire sample.
Convergence of models was assessed using all convergence diagnostics in the CODA package [43], in particular cross-correlations and accuracy of estimating quantiles [44].
Each animal in each experimental group (+3 h, +0 h, and sham pMCAO controls, n = 22 per group, Figure 1M O) was assessed using all three of the following behavioral tests 7 days after pMCAO: the Bederson Neurological Scale [19], [20], forepaw-guided exploration [21], and whisker-guided exploration [22], [23], [24].
The differences in the response variables between spruce logs with tops and branches retained and 4-m spruce logs without tops and branches were assessed using all spruce logs from the 37 experimental blocks containing branched logs (37 branched and 215 branchless logs; only forested sites, not clear-cuts).
Convergence was assessed using all of the Geweke, Raftery-Lewis, Gelman-Rubin and Heidelberger-Welch tests.
Differences in these characteristics were assessed using all datasets with available annotation.
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Sequence identity and similarity shared between protein pairs was assessed using an all-against-all Needleman-Wunsch alignment approach.
Confounding was assessed using an all-possible-subsets approach on covariates eligible for removal (that is, those not statistically significant).
Confounding was assessed using an all-possible-subsets approach on covariates eligible for removal (that is, those not featured in any statistically significant interaction terms or those not statistically significant).
Patient illness severity was assessed using the All-patient refined diagnosis related group (APRDRG) classification within the KID.
Intra-platform reproducibility was assessed using measurements from all available targets.
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