Personalised Mapping of Tumour Development in Synchronous Colorectal Cancer Patients
|Study ID||Alternative Stable ID||Type|
Study Datasets 1 dataset.
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.