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One of the limitations of this analysis is that our PIK3CA mutation assessment was restricted to circulating DNA analysis.
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Despite the obvious appeal of consensus between different analytical methods, a major caveat in using polling strategies for mutation assessment is that these approaches are prone to both systematic and sampling errors.
Therefore, BRAF V600E mutation assessment may be a potentially useful marker in the differential diagnosis of GBM/giant cell GBM vs. "PXA with anaplastic features" and in identifying BRAF V600E mutant astrocytic tumors suitable for targeted therapy.
We predicted these mutations to be viable based on the criteria V2 and V4, and this assessment was experimentally validated.
For the scope of this paper, the qualitative assessment was aimed through the analysis of the test data generated by TeTooDS in relation to mutation criterion.
That assessment was premature.
That assessment was kind.
— The assessment was simple.
Assessment is.
That assessment is wrong.
This assessment is misinformed.
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