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The comparison was done by measuring for each syllable the root mean square error (RMSE) between the synthesized and original utterances.
This observation was quantified by measuring for each cell the ratio of p65 intensity in the nucleus and in the cytoplasm by automated image processing (Figure 1C).
[Ca2+] i was monitored by measuring, for each ROI, the ratio of the mean fluorescence emitted at 510 nm when exciting alternatively at 340 and 380 nm (shortly termed "ratio").
Participants' functions were derived by measuring, for each stimulus, (along the spline function fitted to each individual's UAD – see above) the change in wavelength needed to produce a fixed, criterion change in sensation; these wavelength shifts were averaged across participants to obtain group wavelength-discrimination functions for males and females.
We have observed a clear degradation in accuracy over the length of a run, i.e. when comparing earlier to later flow cycles, by measuring for each flow cycle how much the difference between a flow value and its ideal counterpart (i.e. the closest integer) varies (Fig. 2b).
We next performed a detailed quantitative analysis of the phenotype induced by En activation (the sample size of all experiments is summarised in supplementary material Table S1), by measuring for each embryo the size of the eye field (mean of the two eyes) and the size of the diencephalon, as revealed by the anterior expression domain of pax6 (pat6a) at 1 dpf (Fig. 1C,D).
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The salivary flow and pH were measured for each sample.
Larval sizes were also measured for each colony.
Total gas measured for each sample is equal to 100%%.
Approximately 50,000 events were measured for each sample.
30 plants were measured for each treatment with three replications.
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