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Change in mass of the sample was automatically followed by the microbalance.
The genotype of each sample was automatically determined by measuring allele-specific final fluorescence in an ABI Prism 7900HT Detection System, using SDS 2.3 software for allele discrimination (Applied Biosystems, Foster City, CA, USA).
The change between the first and second slide (stimuli presentation) was controlled by the experimenter, and was dependent on the behavior and attention of the subject (see below for the exact criteria) while the sound sample was automatically played as soon as the visual stimuli appeared.
Each OptiScanner blood sample was automatically withdrawn from a forearm vein.
Quantitation cycle (CQ) for each sample was automatically calculated using the algorithm built in the CFX96 PCR light cycler software.
The concentration of BG in each sample was automatically calculated using a calibration curve with standard solutions ranging from 31.25 to 500 pg/mL.
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The visible spectrum of light, i.e. of wavelength 400 700 nm, was considered, and the absorbance and transmittance of each sample were automatically recorded by the spectrophotometer.
A minimum of six colonies of each sequence and sample were automatically sequenced to determine their degree of methylation.
First, the sample is automatically diluted with a liquid that also lyses the blood cells.
Standard curves, Ct values and copy numbers for each tested sample were automatically generated by the 7500 software.
Intensities of all annotated lipids in each sample were automatically recorded in an Excel sheet using R. Data were normalized with the intensity of the internal standard of each fraction.
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CEO of Professional Science Editing for Scientists @ prosciediting.com