Fig. 2: Variants of interest identified using targeted sequencing of 20 new and known meningioma genes in 76 meningioma blood/tumor pairs. | npj Genomic Medicine

Fig. 2: Variants of interest identified using targeted sequencing of 20 new and known meningioma genes in 76 meningioma blood/tumor pairs.

From: Novel germline and somatic variants in familial and sporadic meningioma genes

Fig. 2

Distribution of 76 variants identified in 76 matched blood/tumor pairs. The variants were identified by targeted sequencing with an average coverage of 805X. Variants were rare (minor allele frequency <0.005) and predicted to be damaging or probably damaging and/or conserved by a consensus of in silico prediction tools. Figure generated using the R statistical software v4.1.1 ggplot2 package in RStudio v1.4.1717.

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