Sentence examples for each sample were calculated from inspiring English sources

Relative abundances of the different taxonomic groups in each sample were calculated.

Average ancestry proportions and 95% confidence intervals for each sample were calculated accounting for both within and between individual variance.

To investigate inter-individual variations in microbial community composition, microbial abundances for each sample were calculated based on the taxonomic assignments of the constituent V1-V5 rRNA gene sequences, followed by normalization across genera.

The weight of the samples was recorded at each step of the procedure, and concentration factors for each sample were calculated based on these records.

Mitochondrial heteroplasmy rates in each sample were calculated as the percentage of the number of alternative reads to that of the total reads.

Once the optical density of the standard and NP samples was matched, the PL spectra were recorded and the relative quantum yields of each sample were calculated using the ratio of the areas under their PL spectra.

For immunostaining results from confocal microscopy, an average number from positively stained cells in a total of six fields of each sample were calculated and average percentages were recorded.

The factor scores for each sample were calculated by normalizing the original variables to standard scores or z values: {text{z }} = left( {{text{x }} upmu } right)/upsigma (1 where μ is the mean and σ the standard deviation for that variable.

The assay was performed in triplicate, and the mean values of each sample were calculated.

Total protein concentrations for each sample were calculated using a BCA protein assay (Pierce), according to the manufacturer's instructions.

Mean fold changes for each sample were calculated by using the 2−ΔΔCt method as previously described [9].