Figure 6.
Figure 6. Analysis of differential gene expression in NrasG12D/+/Tet2+/−HSCs by RNA sequencing. (A) Clustering of differential genes by unsupervised correspondence analysis (COA). (B) List of the top-ranking upregulated and downregulated genes in NrasG12D/+/Tet2+/− vs WT HSCs with a fold change of >2 and false discovery rate (FDR) of <0.1 (P < .05). (C) Quantitative real-time reverse transcription polymerase chain reaction of negative regulators of JAK/STAT signaling in NrasG12D/+/Tet2+/− and WT HSCs from mice 2 weeks post–poly (I:C). Data represent mean ± standard error of the mean. Two-tailed Student t tests were used to assess statistical significance. *P ≤ .05, **P ≤ .01.

Analysis of differential gene expression in NrasG12D/+/Tet2+/HSCs by RNA sequencing. (A) Clustering of differential genes by unsupervised correspondence analysis (COA). (B) List of the top-ranking upregulated and downregulated genes in NrasG12D/+/Tet2+/− vs WT HSCs with a fold change of >2 and false discovery rate (FDR) of <0.1 (P < .05). (C) Quantitative real-time reverse transcription polymerase chain reaction of negative regulators of JAK/STAT signaling in NrasG12D/+/Tet2+/− and WT HSCs from mice 2 weeks post–poly (I:C). Data represent mean ± standard error of the mean. Two-tailed Student t tests were used to assess statistical significance. *P ≤ .05, **P ≤ .01.

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