Barely Significant
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Clonogenic assays improve determination of variant allele frequency of driver mutations in myeloproliferative neoplasms.

Ann Hematol · 2022 · PMC9646600 · PMID 36269400

Europe PMCDOI
1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

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highly significantp < 0.0001actually significant
The calculated clonogenic VAF was lower than the one calculated using NGS of whole blood, but both VAFs showed a highly significant correlation (Fig. 2a ; p < 0.0001).

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