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These models typically require a human-in-the-loop to manually classify sounds which then further train the model on what to look for.
Physics-based machining models typically require significant computational resources and time which makes them impractical for quick process optimization calculations in an industrial shop-floor setting.
To date, implementation of roller compaction models to experimental work has been limited because these models typically require large experimental data sets or obscure input parameters that are difficult to obtain experimentally.
However, these models typically require specifying several input parameter values (such as maximal respiration rates) that are obtained from experimental data and are characterized by high uncertainties due to biological variation.
Future studies would benefit from using growth curve analysis, as this would provide insight regarding both individual and group temporal growth trajectories; however, growth models typically require at least three time points per individual [ 45].
These models typically require free recombination and/or high mutation rates, although evolutionary dynamics at intermediate recombination rates have recently been analysed (Weissman and Barton 2012) and might be transferred to rescue models.
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Here's a quote from the company's CTO, "Training such Deep Neural Net models typically requires large amounts of training data and a high-performance computing environment.
In particular, direct optimization of simulation models, typically, requires a large number of model evaluations, which may be impractical or even infeasible in a reasonable timeframe.
Making these predictions with process-based models typically requires detailed data on the existing tree population structure from which to initiate projection, or alternatively highly complex, and difficult to parameterize, models of inter-tree competition.
However, the most successful of these models typically requires the implantation of multiple human embryonic tissues and are therefore labor intensive and expensive to create[2], [3].
The evaluation of immuno-therapeutic agents in immunodeficient preclinical models typically requires subcutaneous (s.c).
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