Cancer Affected Patients - Data Access Committee

Dr Romy Walker
romy.walker@unimelb.edu.au

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Dataset ID	Description	Technology	Samples
EGAD50000000031	This dataset comprises a genomic and a phenotypic excel sheet displaying 137 cases classified as suspected Lynch syndrome. Included are genotypic data such as tumour mutational burden, tumour mutational signatures and germline/somatic variant calls for each colorectal, endometrial or sebaceous skin tumour screened. Genomic data is derived from targeted multigene panel sequencing including ~300 hereditary cancer genes.	Illumina NovaSeq 6000	137