Analyte losses from the extraction and sample preparation steps are corrected by the isotope dilution analytical technique and should not be significantly greater than the error in the addition of the surrogate internal standard.
After completing data entry, outliers and any missed values were checked using frequency, listing, and sorting and any identified error at any step was corrected by revising the original data abstraction format.
The effective heat of the peptide-metal ion interaction upon each titration step was corrected for dilution and mixing effects, as measured by titrating the divalent metal ion solution into buffer and by titrating buffer into oxytocin solution.
Once the steps are correct, measure two lengths: one out from the standard to where their starting mark is perpendicular and from there to their starting mark.
Absorbance data indicated that less than 10% of the tracer was lost by channeling at the 30% methanol steps; data were corrected for these losses.
In the last step, reflectance values were corrected.
In a second step, the results were corrected for multiple comparisons using cluster-size and cluster-value thresholds obtained by Monte-Carlo simulations using a significance level of p = 0.05.
In the first step, the data were corrected for the disproportionate stratification procedure by assigning to the cases a weight that was the inverse of the sampling fraction of the stratum they had been assigned to.
Steps of the depth were corrected, if necessary, assuming the following priority: the OBS models (highest), the seismicity data, and the inversion of receiver function (lowest).
During the preprocessing step, the sample intensities were corrected for allelic crosstalk, normalized for nucleotide-position probe sequence effects, summarized and finally corrected for the PCR fragment length.
