Study
Matched Ovarian Cancer Sequencing
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001000155 | Cancer Genomics |
Study Description
Genomic libraries (500 bps) will be generated from total genomic DNA derived from 15 ovarian cancer samples and subjected to total of eight lanes of 37 bp, paired end sequencing on the llumina GA. 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 2 datasets.
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 |
|---|---|---|---|
| EGAD00001000050 |
Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes
|
Illumina Genome Analyzer II | 13 |
| EGAD00001000084 |
Matched Ovarian Cancer Sequencing
|
Illumina Genome Analyzer II | 23 |
Who archives the data?
