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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.
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.
Where it is impractical to make a threaded joint tight, a bonding jumper shall be utilized.
It is impractical to block all protons in this way.
Therefore, it is impractical to process large datasets.
Clearly, it is impractical to infect humans with Ad36 to improve diabetes.
It is impractical to transfer this data to the Amazon cloud via a typical network connection.
Due to computational constraints it is impractical to use FLIPS for greater than five markers.
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