Fig. 4: MutSigCV analysis for variant calling. | Blood Cancer Journal

Fig. 4: MutSigCV analysis for variant calling.

From: Genomic insights into the pathogenesis of Epstein–Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon sequencing

Fig. 4: MutSigCV analysis for variant calling.

A Significance levels for all EBV + DLBCL (NOS) MutSigCV genes (P < 0.05) and UpSet plot (B) showing the overlap of MutSigCV genes using EBV + DLBCL (NOS), all-type DLBCL and ABC-type DLBCL data; C shows the overlap between the three tumor entities. D HALLMARK gene sets enrichment for network diffusion analysis of significant MutSigCV genes (MutSigCV P < 0.05).

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