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A comparison of the predicted and observed duration differences is however difficult because the observed differences vary largely across studies (see Figure 3C).
If for some items, the expected observed item score differences can not be explained by differences on a latent level (because the observed differences are too small, or too large, given the difference in latent factor means between the samples), then these items are considered to be biased.
This is because the observed differences not only reflect sequencing errors, which are expected to occur at similar rates across species, but they also reflect true genomic differences between the individuals sequenced for the 2× and ENCODE projects, which will depend on the diversity of the sampled populations, the relatedness of the sampled individuals, and other factors.
Cost-effectiveness and cost-utility analyses of treatments were also recommended, because the observed differences in effectiveness were only small.
Because the observed differences between coding and noncoding phylogenies were statistically significant, our results are indicative of a pattern of convergent evolution at the sequence level.
In addition, significant differences between lipegfilgrastim 6.0 mg and pegfilgrastim were observed for several secondary efficacy measures; however, these data should be interpreted with caution, because the observed differences were small and the clinical relevance has not been confirmed.
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This model was deemed suitable because of the observed differences in settings and populations.
Because of the observed differences in the ATM pathway, we addressed if the activation pattern of the ATM substrate checkpoint kinase 2 (Chk2) was altered in H125 TICs.
Because of the observed differences between ligands and expression patterns associated with TAAR1 as compared to other family members, we performed a branches test to identify if there was a significant difference between the dN/dS values among TAAR1 genes compared to other family members.
Because of the observed differences in EphA2 expression levels, we hypothesized that the level of EGFR siRNA delivery and the subsequent decrease in EGFR expression in the cell lines would depend upon the presence of the EphA2 receptor as well as the concentration of siRNA loaded-nanogels added to the cells.
However, CLSM allowed us to determine the percentage of live/dead bacteria in our isolates, so we believe that this technique is still useful for the study of more detailed aspects of biofilms, although selection of the substrate appears to be important for the study of particular strains, because of the observed differences between them.
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because the observed mortalities
because the observed filaments
because the observed customers
because the observed variables
because the observed lesions
because the observed volumes
because the observed data
because the observed mutations
because the observed assaults
because the observed correlations
because the observed conditions
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