Figure 4.
Quantitative representation of CH clones at different levels of the hematopoietic hierarchy. (A) Sanger sequencing electropherograms exemplifying detection of missense, nonsense, and frameshift mutations in individual CFUs from PB CD34+ cells. (B) Correlation between the percentage of detected mutation-positive CFUs by Sanger and the percentage of predicted mutation-positive CFUs based on VAFs. (C) VAFs in granulocytes, monocytes, B cells, and T cells in donors and recipients shown as a heatmap. (D) VAFs in granulocytes, monocytes, B cells, and T cells in donors and recipients (box and whisker plot). Wilcoxon matched-pairs signed rank test was used to calculate statistical significance.

Quantitative representation of CH clones at different levels of the hematopoietic hierarchy. (A) Sanger sequencing electropherograms exemplifying detection of missense, nonsense, and frameshift mutations in individual CFUs from PB CD34+ cells. (B) Correlation between the percentage of detected mutation-positive CFUs by Sanger and the percentage of predicted mutation-positive CFUs based on VAFs. (C) VAFs in granulocytes, monocytes, B cells, and T cells in donors and recipients shown as a heatmap. (D) VAFs in granulocytes, monocytes, B cells, and T cells in donors and recipients (box and whisker plot). Wilcoxon matched-pairs signed rank test was used to calculate statistical significance.

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