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This method is slow, since molecular beams have low densities of atoms.
There are several numerical methods available for solving these equations; the most common method used for solving such equations is finite difference method; but this method is slow.
The critical threshold has been calculated to high precision for simple geometries using Monte Carlo simulations, but this method is slow at best, and infeasible for complex geometries.
Unfortunately, this method is slow, labor intensive, expensive, and low throughput, rendering it ineffective in public health arenas requiring rapid response.
Therefore, this method is slow and imprecise.
This method is slow, expensive, laborious and low-throughput.
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Table 7 illustrates that when the number of buses is small to moderate (less than 106200), the performance of this method is slower than the best achieved in [7, 9, 12, 33].
For sparsely genotyped data sets it is more accurate to linearly interpolate using LOD scores based on an interval map and derive locus-specific P-values from the interpolated LOD scores, though this method is slower than the one described above.
The major advantage of this method is slower release properties of the capsule and higher throughput rate in comparison to the spray drying process [ 146].
This method is slower than some, but the rebound effect won't happen.
This method was slow, however, and not always successful, as the vintners did not understand the process.
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CEO of Professional Science Editing for Scientists @ prosciediting.com