Study
SCLC
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001000009 | Synthetic Genomics |
Study Description
The aim of this study is to use sequence data generated from 500 bp paired end reads using the Illumina platform to characterise the breakpoints of chromosomal translocations, amplifications and deletions at high resolution (to the bp).
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 |
|---|---|---|---|
| EGAD00001000002 |
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
|
Illumina Genome Analyzer,Illumina Genome Analyzer II | 11 |
Who archives the data?
