Study

Glioma_cell_lines_rearrangement_screen

Study ID Alternative Stable ID Type
EGAS00001000202 Cancer Genomics

Study Description

Genomic libraries (500 bps) will be generated from total genomic DNA derived from 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 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
EGAD00001000090
Glioma cell lines rearrangement screen
Illumina Genome Analyzer II 3

Who archives the data?

There are no publications available