Homo sapiens (ID 340237) - BioProject

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Accession: PRJNA340237 ID: 340237

Homo sapiens (human)

See Genome Information for Homo sapiens

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5 additional projects are components of the VHL deficiency drives enhancer activation of oncogenes in clear cell renal cell carcinoma.

VHL loss is the most common genetic alteration event in ccRCC, but its effect on epigenetic landscape has not been elucidated previously. More...

Accession	PRJNA340237; GEO: GSE86087
Data Type	Epigenomics
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications	Yao X et al., "VHL Deficiency Drives Enhancer Activation of Oncogenes in Clear Cell Renal Cell Carcinoma.", Cancer Discov, 2017 Nov;7(11):1284-1305
Submission	Registration date: 26-Aug-2016 Genome Institute of Singapore
Relevance	Medical

Project Data:

Parameter	Value
Data volume, Supplementary Mbytes	19

Parameter	Value
Data volume, Gbases	126
Data volume, Mbytes	84582

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