Study
Various_Cancer_Fusion_Gene_Sequencing
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001000012 | Cancer Genomics |
Study Description
Genomic libraries (500 bps) will be generated from total genomic DNA derived from 50 commomon epithelial 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 |
|---|---|---|---|
| EGAD00001000002 |
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
|
Illumina Genome Analyzer,Illumina Genome Analyzer II | 11 |
| EGAD00001000005 |
Various Cancer Fusion Gene Sequencing
|
Illumina Genome Analyzer II | 14 |
Who archives the data?
