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Conversely, no significant differences were observed at sensorial level between the samples obtained within our pilot experiment and commercial samples from wild origin.
The statistical analysis indicated significant differences in the positive rates between the samples obtained from areas north and south of the Yangtse River (*P < 0.05), whereas no differences were observed between samples obtained from different genders (P > 0.05).
Matched microarray data was compared between the samples obtained prior to CF treatment and samples collected after resistance to therapy developed.
There is a clear separation between the Northern and Southern samples (open and solid symbols) and well as between the samples obtained from Daphnia acclimated to 18°C vs. 28°C (blue and red symbols; Figure 4A).
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It is important to point out here that, due to the relatively short time span over which the analysed samples were collected (1996 to 2009 but with 95% of the samples obtained between 2000 and 2009), the substitution rates inferred are probably more reflective of short-term mutation rates and not the longer-term substitution rates of EACMV-like viruses [ 15].
The largest difference was observed between samples obtained before feeding and samples obtained 2.5 3.5 h after feeding, while samples obtained 5.0 and 8.0 h after feeding shifted back towards the samples obtained before feeding.
The principal outcome variable was the percent change in outcome of interest between the sample obtained before exposure and the sample obtained 1 or 24 hr later.
Genetic similarity between isolates from DRC and the sample obtained from the 2005 Sudan MPXV outbreak support the second hypothesis, importation of the virus.
Comparison of the fold changes between the two samples obtained by Fluidigm and Affymetrix arrays showed an overall correlation of R = 0.60.
No significant differences were found regarding the impact on conidia germination between the SLS samples obtained from wheat and rice straw.
A ΔCq value was calculated reflecting the difference between the average Cq of the replicate samples obtained for the control gene (18S) and the average Cq of the replicate samples obtained for the test gene to be validated.
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