Figure 2: Mutant allele frequency from deep read count data.
From: Genome remodelling in a basal-like breast cancer metastasis and xenograft
The mutant allele frequency of each somatic mutation is shown. Mutations were validated using both 454 and Illumina sequencing. Each bar represents the average of the frequency yielded by the two technologies for a single primer pair and the error bars represent the standard deviation. Data were considered only if there were at least 200 reads from Illumina sequencing and at least 20 reads from 454 sequencing. If no error bar exists, then data were only available from a single sequencing platform.
