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To explore this possibility, the bacterial operons where divided in two groups according to their Na4vSS values, those with lower and higher aggregation propensity than the mean propensity of the complete operon protein set (−6.4 Na4vSS).
The mean propensity of gene loss for large subunit ribosomal proteins is much lower compared to small subunit ribosomal proteins (Additional file 1: Table S8).
This analysis reveals that the mean propensity of adjacency of mammalian orthologs of weakly imprinted gene pairs in the mouse (parental biases below 85%) is significantly higher than the mean propensity of adjacency of orthologs of all mouse adjacent gene pairs (p-value = 0.007, Figure 5F).
In order to test whether the propensity of adjacency of orthologs of mouse weakly parentally-biased imprinted gene pairs (with a bias lower than 8515%%), is significantly higher than what would be expected by chance, we compared the mean propensity of adjacency of these gene pairs with the mean propensity of adjacency of all gene pairs in the phyletic pattern using a one-sided z-test.
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As there are multiple matches for individuals in the intervention group, the mean propensity scores of matched controls for the corresponding intervention unit, and the propensity score of each intervention unit are illustrated in the figure.
After matching, the all-comparator group had a mean propensity score of 0.340, essentially unchanged for the MMX mesalazine group.
In order to reduce the influence of outlying weights (i.e. those observations with a very high or very low propensity score), weights may be stabilized via multiplication by the mean propensity score of the given exposure group [ 19, 22].
Here, we observe negligible difference in the mean propensity scores and their distribution of the two groups after kernel matching, indicating that we were successful in our matching.
The balancing property of the logit specification is tested to ensure that the sample of invaded households and the sample of non-invaded households have similar mean propensity scores and observables at various levels of propensity scores (Becker and Ichino 2002).
In each case, we measured the: (1) Mean migration propensity of all the cells (pi), (2) Mean maximum migration distance (mi) of all the cells in the neoplasm, and (3) Mean number of cells leaving the edge of the neoplasm (emigrating cells) per time step.
After the selection of 50 controls most closely matching psoriasis individuals based on the propensity score, the mean propensity in the control group score was 0.63 (SD = 0.16), (p = 0.006).
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com