Whole genome sequencing on HiSeq platform of tumour-normal sample pairs from 183 melanoma cases

Dataset ID Technology Samples
EGAD00001003388 N/A 366

Dataset Description

Aligned, merged and deduplicated BAM files from HiSeq whole genome sequencing of 366 samples: matched tumour-normal pairs from 183 melanoma cases comprising 48 primary melanomas, 15 cell lines, and 120 metastases. Sequencing was performed on the Illumina HiSeq 2000 and Xten platforms at Australian and Korean sequencing centres. Data was aligned to the human genome (GRCh37) using BWA-MEM.

Data Use Conditions


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Label Code Version Modifier
ethics approval required DUO:0000021 2019-01-07