Balanced Brain Tumour Whole Genome Sequencing

We propose to definitively characterise the somatic genetics of a number of pediatric malignant tumours including ependymoma, high grade glioma and central nervous system primitive neurectodermal tumours through generation of comprehensive catalogues of somatic mutations by high coverage genome sequencing.

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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
EGAS00001000360 Cancer Genomics
ID File Type Size Located in Quality Control
EGAF00000156239 bam 15.4 GB
EGAF00000156240 bam 19.4 GB
EGAF00000156241 bam 19.6 GB
EGAF00000161409 bam 31.4 GB
EGAF00000161410 bam 31.2 GB
EGAF00000164126 bam 33.5 GB
EGAF00000164127 bam 32.5 GB
EGAF00000164128 bam 31.9 GB
EGAF00000164129 bam 31.8 GB
EGAF00000164130 bam 31.7 GB
EGAF00000164131 bam 32.0 GB
EGAF00000168181 bam 34.7 GB
EGAF00000178136 bam 33.6 GB
EGAF00000178137 bam 31.9 GB
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