The proposed energy threshold selection method often produces better results than the conventional constant threshold as it can remove more interference units, especially the non-speech ones.
However, this method often produces a mixture of orientations with a reduction in binding capacity.
This method often produces antibodies of lower affinity for antigen than the donor antibody.
However, this method often produces a large amount of hazardous solvent waste and is generally cumbersome.
Chemical syntheses of genome can be used to produce very large DNA constructs; however, this method often produces high error rates, and it is very expensive.
The method often produces nonspecific amplification products due to the short arbitrary degenerate (AD) primers and low annealing temperatures, and may also achieve non-efficient amplification of target sequences [ 2, 4].
Standard chemical labeling methods often produced mixed populations of labeled proteins, because the targeted amino acid side chains (thiols, carboxyls, amines) were present more than once in the protein of interest.
Krylov subspace methods often produce the iterates which fluctuate rather strongly.
These measuring methods often produce problems by measurement errors, caused by undesirable heat transport processes that are difficult to control.
Both methods often produce inconsistent results (Gogarten et al. 2002).
