Breast Cancer FRT RNA seq

We propose to definitively characterise the somatic genetics of ER+ve, HER2-ve breast cancer through generation of comprehensive catalogues of somatic mutations in breast cancer cases by high coverage genome sequencing coupled with integrated transcriptomic and methylation analyses.

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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
EGAS00001000420 Cancer Genomics
ID File Type Size Located in Quality Control
EGAF00000163200 bam 5.4 GB
EGAF00000163201 bam 17.6 GB
EGAF00000163202 bam 15.4 GB
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