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Making sense of the prolific range of new compounds produced by new methods still requires clinical testing, and this can yield surprises.
The efficacy demonstrated by these surrogate testing methods still requires validation from clinical practice.
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However, existing hybrid methods still require development of a high-quality unit selection system.
However, conventional PCR based SNP analysis methods still require intact primer binding sites for target amplification.
Although these methods are related to our problem, the direct methods still require a comparatively large amount of images.
Meshless methods still require considerable improvement before they equal the prominence of finite elements in computer science and engineering.
However, as they are bead on symmetric space discretizations, these methods still require the ad hoc tuning of an artificial viscosity to suppress numerical spatial oscillations.
Despite the availability of various methods that can isolate nucleated cells from blood or body fluids, these methods still require centrifugation and other purification devices to work.
But from the reduction methods, only the removal of redundant LUTs can be used as these can be shared together with the flip-flop, while the other methods still require a BLE for a single flip-flop.
However, nearly all current cloning methods still require the introduction of overlaps by PCR, which can introduce undesired mutations.
For the time being, PCR-based methods still require conventional culture being performed because susceptibility testing is paramount in today's emerging resistance.
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