Figure 2.

Distribution of the coverage (horizontal) and the variant allele fraction (vertical) in the tumor exome-seqs. Among the mutations detected by four callers using 16 LUSC tumor-normal exome-seq pairs, mutations detected by a single caller (upper row) or missed by a single caller (lower row) are used. Each column corresponds to a caller that uniquely detects the mutations or uniquely misses the mutations.

Kim and Speed BMC Bioinformatics 2013 14:189   doi:10.1186/1471-2105-14-189
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