Lung_Rearrangement_Study
Genomic libraries (500 bps) will be generated from total genomic DNA derived from cancer samples and subjected to 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.
- Type: Cancer Genomics
- Archiver: European Genome-Phenome Archive (EGA)
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 |
---|---|---|---|
EGAD00001000069 | Illumina HiSeq 2000 | 48 | |
EGAD00001000638 | Illumina HiSeq 2000 | 20 |
Publications | Citations |
---|---|
Processed pseudogenes acquired somatically during cancer development.
Nat Commun 5: 2014 3644 |
64 |