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Thus, in order to provide variant annotation other methods such as functional assays should be used.
Conclusions: While on treatment, qualitative HCV RNA assays should be used to monitor response.
Standard first-line cytotoxicity assays should be performed to ensure biocompatibility.
Nevertheless, to safely exclude pulmonary embolism, D-dimer assays should be combined with other diagnostic tests.
However continuous effort in order to validate and improve clinical reliability of commercially available blot assays should be carried out.
In this context, CTC PD-L1 assays should be tested as a potential 'liquid biopsy' approach for stratification and monitoring of patients with cancer undergoing immune-checkpoint blockade.
It was previously agreed that for regulatory applications, assays should be based upon neutral genes, be generally available in several laboratories, and be readily transferable.
Overall, these robust assays should be valuable for batch-testing clinical material as well as providing tools for improving the design of therapeutic IgG.
We suggest that further assays should be performed using more accurate methods to characterize new molecules with antiviral activity that may result in new drugs.
To confirm this, a correlation analysis of the potencies of NK1 antagonists in the two assays should be performed when further selective NK1 receptor antagonists are available for testing.
We also note that since there exists variability even among some of these markers, these assays should be performed on any newly acquired hMSC population if their bioelectric properties are to be studied further.
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