Burden of Disease in Sarcoma

Study ID Alternative Stable ID Type
EGAS00001000087 Cancer Genomics

Study Description

Genomic libraries (500 bps) will be generated from total genomic DNA derived from cancer samples and subjected to 50 bp, paired end sequencing on the llumina HiSeq 2000. 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
Burden of Disease in Sarcoma
Illumina HiSeq 2000 220

Who archives the data?

There are no publications available