Genomic Oncology Research Group DAC

simonfurney@rcsi.ie

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Dataset ID	Description	Technology	Samples
EGAD00001006131	Here, we performed a characterisation of 12 tumours and matched normal samples from 3 syCRC patients by whole genome sequencing: Patient A (tumours A1 and A2), Patient B (tumours B1-B5), and Patient C (tumours C1-C5). Somatic SNVs, indels and stuructural variants were called.		3