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Both methods are hard to scale up.
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It is just that the problem general methods are hard to solve.
Especially, these methods are hard to be reused to generate the mid-surface model efficiently.
However, these methods are hard to be implemented and mostly time consuming and they strongly relate to the proposed models and applications.
These methods are hard to implement in radio frequency IPSs because very accurate timers are needed to reach an acceptable accuracy.
Subjectively, the results of these two methods are hard to distinguish (Fig. 9; images of Building and Lena; and Fig. 10).
Least-squares methods are hard models and require knowledge about the chemistry of the reaction system, i.e., an initial set of stoichiometric coefficients and stability constants for the postulated species.
Since the existing methods are hard to satisfy the accuracy and speed requirements of engineering applications, we propose to estimate crowd density by an optimized convolutional neural network (ConvNet).
The other difficulty with this section is that the methods are hard to follow.
The idea that lineage-tracing methods are hard to apply in human cells should be stated, as everything else hinges on numerical arguments on cleanliness of cell separations, etc. chgA is an endocrine differentiation marker.
The idea that lineage-tracing methods are hard to apply in human cells should be stated, as everything else hinges on numerical arguments on cleanliness of cell separations, etc.
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