Sentence examples for for each transcript were normalized to from inspiring English sources

(2007), mRNA reads densities from 5, 24 and 72h for each transcript were normalized to 1, and hierarchical clustering based on Euclidian distance was performed using Cluster 3.0.

Uniquely mapped tag counts for each transcript were normalized to TPM to facilitate comparison between different samples.

Fold change was calculated using the comparative Ct (ΔΔCt) method where values for a particular transcript were normalized to an endogenous control within each sample (act-1 mRNA levels) and then normalized to the calibrator sample (control RNAi gonads).

For each experimental sample, the amount of specific transcript was normalized to the amount of act1 transcript measured in the same sample.

For quantitative analysis of gene expression, the target transcripts were normalized to the number of flaB transcripts, whereas for quantitative measurement of B. burgdorferi burden in infected tissues, flaB transcripts were normalized to mouse or tick β-actin levels.

The expression levels of interest transcripts were normalized to the housekeeping PPIA (peptidylprolyl isomerase A) transcripts.

The expression levels of interesting transcripts were normalized to the housekeeping β2 microglobulin (B2M) and PPIA gene transcripts.

Finally, the mRNA levels of each transcript were normalized with those of the corresponding CYP2 transcript.

All samples were run in triplicate and bteA transcript (P1 + P2 transcripts) was normalized to the recA transcript for each sample.

The mean threshold cycle (CT) value for each transcript was normalized by dividing it by the mean CT value for the β-actin transcript for that sample.

The relative abundance of the transcripts was normalized to the CD3ε transcript.