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Genomic characterisation of SDH deficient renal cell carcinoma - RNA

SDH deficient renal cell carcinomas are a rare and recently defined subtype of kidney cancer, often associated with an inherited mutation in one of the SDH gene subunits. This dataset sought to understand the genomic events that underpin tumour formation, from putative cell of origin, characterisation of the tumour microenvironment, to the genomic evolution of these rare tumours. We performed whole genome and RNA sequencing of 4 patients with SDH deficient renal cell carcinomas, including one patient who had an additional paraganglioma. An addition patient in this cohort had the initial diagnosis revised to a clear cell renal cell carcinoma.

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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.

Study ID Study Title Study Type
EGAS00001004103 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00005765576 cram 1.6 GB
EGAF00005765577 cram 1.4 GB
EGAF00005765578 cram 1.8 GB
EGAF00005765579 cram 1.9 GB
EGAF00005765580 cram 2.1 GB
EGAF00005765581 cram 1.9 GB
EGAF00005765582 cram 2.7 GB
EGAF00005765583 cram 1.8 GB
EGAF00005765584 cram 2.3 GB
EGAF00005765585 cram 2.1 GB
EGAF00005765586 cram 1.6 GB
EGAF00005765587 cram 1.4 GB
EGAF00005765588 cram 1.7 GB
EGAF00005765589 cram 1.9 GB
EGAF00005765590 cram 2.0 GB
EGAF00005765591 cram 1.8 GB
EGAF00005765592 cram 2.6 GB
EGAF00005765593 cram 1.8 GB
EGAF00005765594 cram 2.2 GB
EGAF00005765595 cram 2.0 GB
20 Files (38.5 GB)