Bone Cancer - Rare Types Whole Genome
We propose to definitively characterise the somatic genetics of a selection of rare bone cancers through generation of comprehensive catalogues of somatic mutations by high coverage genome sequencing.
- Technology: Illumina HiSeq 2000
- 33 samples
- DAC: EGAC00001000010
Studies are experimental investigations of a particular phenomenon. e.g. case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients. Click on one of the Study IDs below to find out more.
|Study ID||Study Title||Study Type|