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Data normalization was accomplished using the endogenous control (β-actin) and the normalized values were subjected to a 2-ΔΔ Ct formula to calculate the fold change between the control and experiment groups.

Normalization was accomplished employing Rp49 and gapdh as housekeeping genes.

After scanning, intensity data were extracted from images, and within-array normalization was accomplished using manufacturer-provided software (NimbleScan).

In each case, the normalization was accomplished by dividing by the BOLD response associated with the preferred visual field location.

Retention time normalization was accomplished in two steps: a primary alignment using the internal standard peptides and a secondary fine tuning using all of the common features.

Normalization was accomplished by LC-MS profiles (normalization based on total MS derived total ion-current area as an estimate of total protein content).

The rescaling (normalization) is accomplished by the linear interpolation formula given in Equation 9.

Both within-slide and inter-slide normalization were accomplished: in this fashion, local distortions in signal and background intensity within different regions of a slide, as well as overall differences in hybridization or labeling efficiencies between slides, were overcome.

In a prospective audit of FFP transfusion in patients with mild PT prolongation (13 17 s), halfway normalization of PT was accomplished in only 15% of cases and full correction in <1%.

Normalization of gene expression data was accomplished in two ways: per chip normalization and per gene normalization.

Normalization of gel bands was accomplished by analysis of two wavelengths, where α-tubulin, CDC-2 or phospho-histone H3 was used as loading control.