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. 2015 Dec 17;18(3):379–387. doi: 10.1093/neuonc/nov289

Fig. 2.

Fig. 2.

Boxplot demonstrating the range of coverage depth values for known (hot spot) variants detected in 30 genes in GlioSeq next-generation sequencing panel. Horizontal line indicates the threshold for minimum coverage (300x) for reporting sequence variants.