Study

Osteosarcoma whole genome rearrangement screen

Study ID Alternative Stable ID Type
EGAS00001000330 Cancer Genomics

Study Description

Genomic libraries (500 bps) will be generated from total genomic DNA derived from Osteosarcoma cancer patients and subjected to short paired end sequencing on the llumina platform. 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.

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Dataset ID Description Technology Samples
EGAD00001000368
Genomic libraries (500 bps) will be generated from total genomic DNA derived from Osteosarcoma cancer patients and subjected to short paired end sequencing on the llumina platform. 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.
Illumina HiSeq 2000 3

Who archives the data?

There are no publications available