Cell_Line_Sub_Clone_Rearrangement_Screen

Genomic libraries (500 bps) will be generated from total genomic DNA cancer samples and subjected to 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: EGA European Genome-Phenome Archive

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
EGAD00001000064	Cell Line Sub Clone Rearrangement Screen	Illumina Genome Analyzer II	6
EGAD00001000154	Single-cell genome sequencing reveals DNA-mutation per cell cycle	Illumina Genome Analyzer II Illumina HiSeq 2000	12