Study
Burden of Disease in Sarcoma
Study ID | Alternative Stable ID | Type |
---|---|---|
EGAS00001000087 | Cancer Genomics |
Study Description
Genomic libraries (500 bps) will be generated from total genomic DNA derived from cancer samples and subjected to 50 bp, paired end sequencing on the llumina HiSeq 2000. Paired reads will be mapped to build 37 of the human reference genome to facilitate the generation of genome wide copy number information, and the identification of novel rearranged cancer genes and gene fusions.
Study Datasets 1 dataset.
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Dataset ID | Description | Technology | Samples |
---|---|---|---|
EGAD00001000127 |
Burden of Disease in Sarcoma
|
Illumina HiSeq 2000 | 220 |
Who archives the data?
