Ewings Sarcoma Rearrangement Screen

Cancer is driven by mutations in the genome. We will uncover the mutations that give rise to Ewing's sarcoma, a bone tumour that largely affects children. We will use second generation Illumina massively parallel sequencing, and bespoke software, to characterise the genomes and transcriptomes of Ewing's sarcoma tumours.

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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
EGAS00001000362 Cancer Genomics
ID File Type Size Located in Quality Control
EGAF00000166464 bam 16.2 GB
EGAF00000166465 bam 12.7 GB
EGAF00000166466 bam 16.8 GB
EGAF00000166467 bam 14.9 GB
EGAF00000166468 bam 15.3 GB
EGAF00000166469 bam 28.3 GB
EGAF00000166470 bam 36.4 GB
EGAF00000167240 bam 16.0 GB
EGAF00000167241 bam 13.6 GB
EGAF00000167242 bam 13.4 GB
EGAF00000167243 bam 17.5 GB
EGAF00000167244 bam 18.0 GB
EGAF00000167245 bam 13.0 GB
EGAF00000167246 bam 14.2 GB
EGAF00000167247 bam 16.2 GB
EGAF00000167248 bam 16.8 GB
EGAF00000167249 bam 26.5 GB
EGAF00000170935 bam 34.7 GB
EGAF00000188429 bam 29.7 GB
EGAF00000188430 bam 25.8 GB
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