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Distinguishing between these three steps is useful in identifying the pathways through which market interventions can affect population health and in assessing how to quantify population health impact.
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In cell models, the ratio of activities of these three steps will vary between different cell lines and different clones.
We alternate between these two steps until convergence.
Our main improvement is embedding the SUSC between these two steps.
Iteration between these two steps increases the joint likelihood until convergence is reached.
A link procedure for fitting the cross sections is developed between these two steps.
The EM algorithm iterates between these two steps and converges to a local maximum of the likelihood.
The path between these two steps is not fully understood; however, variables such as pressure, temperature, composition, and the velocity generally influence this process.
The algorithm cycles between these two steps back and forth.
Between these two steps cDNA was cleaned using MSB Spin PCRapace kit (Invitek, Germany), following manufacturers' protocol.
We observed a 32% increase in mean TSNR between these two steps, demonstrating the importance of such regressors to characterize and remove structured noise sources.
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