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The integrated intensity was divided by average integrated intensity of neuronal cells to obtain ratio of DNA content of each cell with respect to the DNA content of neurons.
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Agilent scanner was used to obtain ratios of Cy5/Cy3 signals from the targets localized on the array.
The estimated differences in the ln scale were consequently exponentiated to obtain ratios of the medians, which are presented later.
C-labelling was utilised to obtain ratios of intracellular fluxes at the metabolic branching points [ 23, 43].
The amplitudes difference of the obtained ratio spectrum at 263.6 nm (λiso) and 240 nm were recorded (∆Pm).
Any inscattering is assumed to be equal to the two VOIs; however, this will lower the ratio between the two VOIs, which may further underestimate the obtained ratio.
Since the obtained ratio t = 1.499 is less than the critical one (t < t n (P)), the value 10.090 should not be excluded at reliability P = 0.99.
For MET, the scanned spectra of its prepared solutions were divided by the normalized spectrum of MEH and the obtained ratio spectra were mean centered.
The obtained ratio was normalized with the ratio of the corresponding cell numbers.
False negatives could be obtained (ratio = 1).
The obtained ratio was named as Rmir (Rmir = N > Benign/N < Benign).
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