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. 2019 Jan 1;9(2):540–553. doi: 10.7150/thno.28374

Figure 2.

Figure 2

Frequently mutated genes in HMCLs shared with MM patients at diagnosis and relapse. Exome-seq data of 59 MM patients including 43 newly diagnosed and 16 relapsing were processed with the analysis workflow. (A) Oncoplot of frequently mutated genes in HMCLs (N >= 5) shared with patients at diagnosis. (B) Oncoplot of frequently mutated genes in HMCLs (N ≥ 5) shared with patients at relapse. Eleven patients without detectable mutations were not included in the figure. N is the number of patients mutated for a given gene.