Matched_Ovarian_Cancer_Sequencing

Genomic libraries (500 bps) will be generated from total genomic DNA derived from 15 ovarian 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.

Type: Cancer Genomics
Archiver: European Genome-Phenome Archive (EGA)

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
EGAD00001000050	Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes	Illumina Genome Analyzer II	13
EGAD00001000084	Matched Ovarian Cancer Sequencing	Illumina Genome Analyzer II	23