Myelodysplastic Syndrome Follow Up Series

Dataset ID Technology Samples
EGAD00001000283 Illumina HiSeq 2000 764

Dataset Description

Agilent whole exome hybridisation capture was performed on genomic DNA derived from MDS and matched normal DNA from the same patients. Next Generation sequencing performed on the resulting exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes. Now we aim to discover the prevalence of our findings using bespoke pulldown methods and sequencing the products from a larger set of patient DNA.

Data Use Conditions


See further information on Data Use Conditions

Label Code Version Modifier
general research use DUO:0000042 2019-01-07
not for profit, non commercial use only DUO:0000018 2019-01-07
health or medical or biomedical research DUO:0000006 2019-01-07
project specific restriction DUO:0000027 2019-01-07