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The viability of our method for biological sample assays was demonstrated by measuring the miRNA-21 contents in three human serum samples.
The obtained results confirm the viability of our method and indicate that it can adapt the internal map representation over time to localize the robot both globally and locally.
This choice thus imitates a scenario in which some 80/180 = 44% of the data is labeled (where we consider that the test set is used here only for purposes of evaluating the viability of our method).
We confirmed the viability of our method using five different cell lines, breast cancer cells (BT20), mouse normal embryonic fibroblast (NEF) as well as those expressing E6/E7 onco-proteins of human papillomavirus (HPV) type 16, and a human cervical cancer cell line (HeLa).
This is also an important control to establish the viability of our method.
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Computational results on this testbed show the viability of our methods, proving that savings in the order of millions of Euro can be achieved.
Further, multi-center studies are needed to determine the viability of our estimation method in PET facilities with various clinical circumstances.
To validate the method, the viability of our corticostriatal organotypic slice cultures was analyzed using a standardized protocol for PI uptake.
The viability of the method is illustrated by using nonlinear engineering problems.
This paper demonstrates the viability of the method for low-strength mortar characterization.
Numerical examples are presented to show the viability of the method.
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