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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.

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