Cancer Exome Resequencing

Study ID Alternative Stable ID Type
EGAS00001000206 Cancer Genomics

Study Description

Genomic libraries (500 bps) will be generated from total genomic DNA derived from a range of cancer samples and subjected 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
Cancer Exome Resequencing
Illumina Genome Analyzer II 58
The landscape of cancer genes and mutational processes in breast cancer
Illumina Genome Analyzer II,Illumina HiSeq 2000 199

Who archives the data?