Serosal (Cs) and mucosal (Cm) FITC concentrations were corrected respectively for dilution and flux.
Remember and know judgments, corrected respectively for remember and know false alarms, were also analysed.
The probability values for voxel and cluster thresholds were 0.005 (uncorrected) and 0.05 (corrected), respectively.
In the following, 's' denotes the normal Sr standard, 't' denotes the Sr spike, and 'm' and 'c' represent the measured and corrected values, respectively.
The dash and thick lines represent the uncorrected and conformance corrected data, respectively Open image in new window Fig. 11 Normalised pore-size distribution (PSD) for samples 6 and 7.
The dash and thick lines represent the uncorrected and conformance corrected data, respectively Open image in new window Fig. 9 Normalised pore-size distribution (PSD) for samples 3 and 4 Open image in new window Fig. 10 Plots of capillary pressure versus mercury saturation for the carbonate core samples 6 and 7.
Shown are the differences between uncorrected and corrected SURs, respectively, and the SURs measured at T=55 min. (A) Absolute difference at T=20 min. (B) Fractional difference at T=20 min. (C) Absolute difference at T=35 min. (D) Fractional difference at T=35 min. Figure 5 Absolute and fractional differences of SUVs in the dynamic data.
Shown are the differences between uncorrected and corrected SUVs, respectively, and the SUVs measured at T=55 min. (A) Absolute difference at T=20 min. (B) Fractional difference at T=20 min. (C) Absolute difference at T=35 min. (D) Fractional difference at T=35 min. The corresponding results for the DTP data are presented in Figure 6 (SUR) and Figure 7 (SUV).
When only the top 20 SNPs were again selected, PVE was improved by 8.4%and7.6%6% for the uncorrected and corrected models, respectively.
Upon corrections for multiple testing, however, only MIP-1α and IL-1α remained negatively correlated with clot strength (r=−0.730 and −0.686; corrected p=0.012 and 0.024, respectively) and overall coagulability (CI; r=−0.640 and −0.648; both corrected p=0.048; figure 1).
For both activity assays, the spontaneous formation of the measured reaction product and its potential presence in protein preparations was corrected by respectively non-enzyme controls and zero time point controls.
