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Weighted Consolidation first orders pathway pairs by scores that incorporate information about the number of overlapping resultant genes and the interactions among those resultant genes.
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Kinetic study reveals that the adsorption follows first order pathway.
These cells provide input to two parallel pathways that process variations in local luminance (first-order pathway) and local contrast (second-order pathway).
These studies suggest an ordered pathway for the assembly of promoter chromatin architecture.
The latter will increase the surface area allowing for more QD loading and for an ordered pathway for faster electron transport.
The results of the kinetic analysis suggest that the main contribution to the zero-order pathway is due to the features of the catalyst surface and the transport of catalyst grains from water to the organic phase.
Ra and Rb follow second-order annihilation kinetics, while the decay of the radical Rc is comprised of at least two parallel kinetic processes, a slow second-order pathway and a fast pathway which can be equally well fitted to first- or second-order kinetics.
For the ANOVA, the genes were nested factors within the higher order pathway.
It has been described as an ordered pathway, with initial cleavage by aspartic proteases followed by action of other proteases, eventually leading to free amino acids [12].
An important tool for ordering pathway components is genetic epistasis analysis, and here we present a strategy termed Alternative Inputs (AIs) to perform systematic epistasis analysis.
The series of events that drives auto-activation of PR and maturation of RT and IN also follows a sequential and ordered pathway, beginning with the p2-NC cleavage [40].
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