Cell Line Sub Clone Rearrangement Screen

Study ID Alternative Stable ID Type
EGAS00001000178 Cancer Genomics

Study Description

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.

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

Who archives the data?