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The period sensitivity was less than the amplitude sensitivity.
For a high CV period (CV period order >300) the period sensitivity distributions were varied because they belonged to all the clusters.
Since the CVs of period were hardly correlated with those of amplitude (Figure S6) and the period sensitivity distributions were different from the amplitude ones, the mechanisms providing robust properties to period and amplitude are different.
On the other hand, a maximum value of period sensitivity was more than 0.3 (7.2 h) with respect to some kinetic parameters, indicating that not only network structures but also parameter values are critical for generating a robust cycle.
However, the period sensitivity of KdCn, despite lying close to the x-axis, remains identifiable, indicating a robust prediction.
In the post term period sensitivity and specificity range from 68 96 % and 52 97 % respectively [ 78, 81].
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Our interpretation of this is a hypothesis of two sensitive periods: sensitivity (to manual socioeconomic position) in childhood and sensitivity to change (from nonmanual to manual socioeconomic position) in adulthood.
We compute the period sensitivities in standard electrical circuit models and find that an increase in one sensitivity can be accompanied by a decrease in another sensitivity.
Relative period sensitivities were integrated into the bootstrap method by calculating appropriate sensitivities for each estimated parameter set.
Since adjustments to periodic systems in response to inputs are often manifested through temporary changes in oscillatory period, relative period sensitivities, (4) ∂ ln T ∂ ln p were calculated due to their independence of parameter magnitude [ 12, 23, 24].
Molecular breeding strategies are increasingly being adopted to develop genetic linkage maps and to identify genomic regions influencing traits of importance in sorghum, e.g. stay-green [ 6] fertility restoration [ 7], ergot resistance [ 8], midge resistance [ 9] and photo-period sensitivity [ 10, 11].
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