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Theoretically, complete genome coverage with no enrichment would be result in a trace with a slope equal to one that intersects the origin (eg: whole genome sequencing wherein 50% of the genome is contains 50% of all aligned reads).
We chose not do this because it introduces a second fitting parameter in addition to γi, which is adjusted to yield a theoretical slope equal to one in Equation 15.
Estimates of ΔΩr,m for the formation of the diffuse layer species (>SOH...M2+) from ΔΩr,m and a theoretical slope equal to one did not reproduce the limited data for this reaction.
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In both cases, Affymetrix and Incyte, the data fit a straight line with slope approximately equal to one and intercept near zero.
The relationship between effective FL and LMTU was almost linear with a slope equal to 0.49 ± 0.06 (r2 = 0.52 to 0.97).
The straight lines were obtained with slope equal to ((- Delta H_{text{ads}}^{^circ } / 2. 30 3 {text{ R}})).
Each trophic link that has a slope equal to −1 (−45°) has consumer and resource of equal biomass B, a characteristic trait of steady-state systems.
The line connecting these points has a slope equal to the risk difference: (0.4-0.2)/(1-0.2= 0.2.
* With calibration slope equal to 1 (i.e. calibration in the large).
Accordingly, ln [1/(1─ P f )] vs. ln (strength) will yield a slope equal to the Weibull modulus (m) [ 21, 22].
They corresponded to the position where the slope of the ROC curves was equal to one.
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