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Linear regression lines

Using a hand calculator, find the slope of the linear regression line that passes through the origin and best satisfies the points... [Pg.63]

Figure 2.4. Graph of the linear regression line and data points (left), and the residuals (right). The fifty-fold magnification of the right panel is indicated the digital resolution 1 mAU of a typical UV-spectrophotometer is illustrated by the steps. Figure 2.4. Graph of the linear regression line and data points (left), and the residuals (right). The fifty-fold magnification of the right panel is indicated the digital resolution 1 mAU of a typical UV-spectrophotometer is illustrated by the steps.
Figure 2.9. The confidence interval for an individual result CI( 3 ) and that of the regression line s CLj A are compared (schematic, left). The information can be combined as per Eq. (2.25), which yields curves B (and S, not shown). In the right panel curves A and B are depicted relative to the linear regression line. If e > 0 or d > 0, the probability of the point belonging to the population of the calibration measurements is smaller than alpha cf. Section 1.5.5. The distance e is the difference between a measurement y (error bars indicate 95% CL) and the appropriate tolerance limit B this is easy to calculate because the error is calculated using the calibration data set. The distance d is used for the same purpose, but the calculation is more difficult because both a CL(regression line) A and an estimate for the CL( y) have to be provided. Figure 2.9. The confidence interval for an individual result CI( 3 ) and that of the regression line s CLj A are compared (schematic, left). The information can be combined as per Eq. (2.25), which yields curves B (and S, not shown). In the right panel curves A and B are depicted relative to the linear regression line. If e > 0 or d > 0, the probability of the point belonging to the population of the calibration measurements is smaller than alpha cf. Section 1.5.5. The distance e is the difference between a measurement y (error bars indicate 95% CL) and the appropriate tolerance limit B this is easy to calculate because the error is calculated using the calibration data set. The distance d is used for the same purpose, but the calculation is more difficult because both a CL(regression line) A and an estimate for the CL( y) have to be provided.
Figure 2.19. Intersection of two linear regression lines (schematic). In the intersection zone (gray area), at a given c-value two PD-curves of equal area exist that at a specific y-value yield the densities zi and Z2 depicted by the dashed and the full lines. The product zi Z2 is added over the whole y-range, giving the probability-of-intersection value for that x. The cumulative sum of such probabilities is displayed as a sigmoidal curve the r-values at which 5, respectively 95% of Z2) s reached are indicated by vertical arrows. These can be... Figure 2.19. Intersection of two linear regression lines (schematic). In the intersection zone (gray area), at a given c-value two PD-curves of equal area exist that at a specific y-value yield the densities zi and Z2 depicted by the dashed and the full lines. The product zi Z2 is added over the whole y-range, giving the probability-of-intersection value for that x. The cumulative sum of such probabilities is displayed as a sigmoidal curve the r-values at which 5, respectively 95% of Z2) s reached are indicated by vertical arrows. These can be...
The trend logio(CV) vs logjo(c) appears reasonably linear (compare this with Ref. 177 some points are from the method validation phase where various impurities were purposely increased in level). A linear regression line B) is used to represent Ae average trend (slope = -0.743). The target level for any given impurity is estimated by a simple model. Because the author-... [Pg.196]

Figure 4.26. Shelf-life calculation for active components A and B in a cream see data file CREAM.dat. The horizontals are at the j = 90 (specification limit at t = shelflife) resp. y = 95% (release limit) levels. The linear regression line is extrapolated until the lower 90%-confidence limit for Kfl = a + h x intersects the SLs the integer value of the real intersection point is used. The intercept is at 104.3%. Figure 4.26. Shelf-life calculation for active components A and B in a cream see data file CREAM.dat. The horizontals are at the j = 90 (specification limit at t = shelflife) resp. y = 95% (release limit) levels. The linear regression line is extrapolated until the lower 90%-confidence limit for Kfl = a + h x intersects the SLs the integer value of the real intersection point is used. The intercept is at 104.3%.
Purpose Calculate the intersection of two linear regression lines and estimate the 95% confidence limits on the intersection coordinate. (See Fig. 2.19.)... [Pg.374]

For the basic evaluation of a linear calibration line, several parameters can be used, such as the relative process standard deviation value (Vxc), the Mandel-test, the Xp value [28], the plot of response factor against concentration, the residual plot, or the analysis of variance (ANOVA). The lowest concentration that has been used for the calibration curve should not be less than the value of Xp (see Fig. 4). Vxo (in units of %) and Xp values of the linear regression line Y = a + bX can be calculated using the following equations [28] ... [Pg.249]

To begin, the following summation notation may be used to calculate the slope (kj) of a linear regression line given a set of X, Y paired data (equation 61-23). [Pg.399]

The elimination constant for a chemical in plasma. Typically calculated using the formula Kel = — ln[10] x b where b is the slope of the linear regression line of the log of the mean plasma concentrations vs. time from the tmsx to 24 hours. [Pg.695]

Figure 4. Calculated activation energies AE vs. o (0-O) orbital energies (averaged in case of 2a and 2b). Linear regression line derived from the model complexes 2a. Figure 4. Calculated activation energies AE vs. o (0-O) orbital energies (averaged in case of 2a and 2b). Linear regression line derived from the model complexes 2a.
When I calculated the estimated amount interval from only the response dispersion for the data using Kurtz methods, there was a substantial reduction in the amount bandwidth from the total bandwidth. This calculation was done by intersecting the bounds of the response dispersion with the linear regressed line and projecting these points to the amount axis. This reduction, however, was not nearly enough to account for differences from Wegscheider s calculation to the others. In Table IV the data is... [Pg.191]

As shown in Table VII there appears to be no significant change of k with respect to temperature. These data were plotted using Equation 3 and from linear regression analysis, the heat of solution was tO.IE Kcal/mole. Since Ah should be negative, this low value is obviously caused by experintental error. Furthermore, the Ah calculated from the standard error of the estimate (t1 standard deviation units) of the linear regression line is +0.17 Kcal/mole. Since Ah is zero or is very close to zero. Equation 3 reduces to... [Pg.215]

Figure 17.3 Tier 1 myeloid assay (Ml cell line) evaluate in-house were compared to IC50 qualification using known hematotoxicants of from level 1 myeloid cell assay, n — 3 different chemical pharmacology and structure, experiments with triplicate wells within each Fifteen compounds with either known colony- experiment. The linear regression line is forming unit granulocyte-macrophage plotted showing the correlation between the... Figure 17.3 Tier 1 myeloid assay (Ml cell line) evaluate in-house were compared to IC50 qualification using known hematotoxicants of from level 1 myeloid cell assay, n — 3 different chemical pharmacology and structure, experiments with triplicate wells within each Fifteen compounds with either known colony- experiment. The linear regression line is forming unit granulocyte-macrophage plotted showing the correlation between the...
The linear regression line to the data in Table 9.1 is given in Fig. 9.2. [Pg.182]

The concentration of the CSF analyte is calculated by interpolation of the observed analyte IS peak-area ratio into the linear regression line for the calibration curve, which is obtained by plotting the peak-area ratios against analyte concentration. [Pg.121]

As a calibration procedure in ICP-MS via calibration curves, external calibration is usually applied whereby the blank solution is measured followed by a set of standard solutions with different analyte concentrations (at least three, and it is better to analyze more standard solutions in the same concentration range compared to the sample). After the mass spectrometric measurements of standard solutions, the calibration curve is created as a plot of ion intensities of analyte measured as a function of its concentration, and the linear regression line and the regression coefficient are calculated. As an example of an external calibration, the calibration curve of 239 Pu+ measured by ICP-SFMS with a shielded torch in the pgC1 range is illustrated in Figure 6.15. A regression... [Pg.193]

Figure 4.1 plots the temporal changes in the number of new molecular entities (U.S. FDA 2005). Although short-term trends are "noisy," there is a clear upwards trend in the data as defined by the linear regression line. [Pg.42]

Figure 9.11 Plot of log Kioc versus log Klaw for PAHs ( ) and for a series of alkylated and chlorinated benzenes and biphenyls (PCBs) (A). The slopes and intercepts of the linear regression lines are given in Table 9.2. Figure 9.11 Plot of log Kioc versus log Klaw for PAHs ( ) and for a series of alkylated and chlorinated benzenes and biphenyls (PCBs) (A). The slopes and intercepts of the linear regression lines are given in Table 9.2.

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