MDSMPN Rearrangement Screen

Study ID Alternative Stable ID Type
EGAS00001000034 Cancer Genomics

Study Description

Genomic libraries (500 bps) will be generated from total genomic DNA derived from 11 Myelodysplastic Myeloproliferative neoplasms (MDSMPN) and subjected to total of two lanes of 50 bp, paired end sequencing on the llumina HiSeq. 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
MDSMPN Rearrangement Screen
Illumina HiSeq 2000 11

Who archives the data?

There are no publications available