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It is impractical to identify effective drug combinations by large-scale drug screening experiments, since the number of combinations increases exponentially with the number of screened drugs.
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First, it would be impractical to identify all fungi sampled, and second there is no reason to expect that pathogens and non-pathogens differ in their abiotic requirements for growth.
Unlike the ME algorithms with fixed search ranges, for example, the full search algorithm, it is impractical to precisely identify the number of computational steps for ACQPPS.
Because of its rarity, it is impractical to perform reflex screening IHC on all renal cancers.
High-throughput screening is useful to identify possible drug combinations; however, it is impractical to screen all possible drug combinations for all possible indications.
It is impractical to charge for these individually.
Therefore, it is impractical to simulate all hundreds of SAGD realizations.
Thus, it is impractical to use it as a detector for the class of PSK signals.
It is impractical to have two expressions depending on the reliability index β.
It is impractical to process this volume of information in the context of infrastructure asset management.
However, it is impractical to use them for twist optimization due to the high computational cost.
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