Whole genome sequencing on HiSeq platform of tumour-normal sample pairs from 183 melanoma cases
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.
- 26/06/2017
- DAC: EGAC00001000010
ICGC Data Access
Please use the ICGC website for applying for access to the data: https://ega-archive.org/dacs/EGAC00001000010
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| EGAS00001001552 | Other |