The entire coding regions of fifty-seven genes were included in a hybridisation capture panel (Supplementary File 1_Table 1), based on: recurrence in our WES tumour set; reported in the Catalogue of Somatic Mutations in Cancer (COSMIC) database; implicated in cancer65 (link); or reported in the TCGA or Bueno et al. studies4 (link),5 (link). Sequencing libraries were prepared from DNA extracted from tumours and normal tissue (whole blood) samples using the SureSelect QXT Target Enrichment System (Agilent, Santa Clara, USA) according to the manufacturer`s protocols. Sequencing was performed on a MiSeq or NextSeq500/550 platform (Illumina) with a mean read depth of 780.6X (all samples). Supplementary File 2_Table 3 contains a list of filtered somatic variants from targeted capture sequencing.
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