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These characteristics would be called the variables of the study, and data values for each of the variables would be associated with each individual.
Data values for each sample were normalized between the two platforms against the median of normal breast SAGE libraries, and Log2-based expression ratios were obtained.
The ELISA raw data values for each sample were used to calculate the percent antibody remaining bound in the presence of 3 M ammonium thiocyanate as compared to phosphate buffer (i.e., 0 M ammonium thiocyanate).
The means of six data values for each treatment were calculated.
Raw data values for each gene were natural-log transformed, median-centered, and quantile-normalized across all arrays.
The actual data values for each PCR, compared to that of the microarray experiment are shown in Table 2.
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The data value to be transmitted from a correlator node is selected as 100 plus a random differential data value for each data gathering.
When one updates data in and MDB the hypertable also changes the data values for all rows and for each time interval.
For each coefficient, data values for all image categories were normalized to the interval [0,1].
Parameters are estimated from a set of n experiments, each with data values for a i (substrate), b i (product), v i (reaction rate), for experiment i.
Initially the two data values required for each task are text title or description and task duration.
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