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Accession: PRJNA253483 ID: 253483

Homo sapiens (human)

Retinoblastoma genome methylation data

See Genome Information for Homo sapiens
Retinoblastoma is the most common intraocular cancer of infancy and childhood, with an incidence of one case per 15,000 - 20,000 live births. More...
AccessionPRJNA253483; GEO: GSE58783
Data TypeEpigenomics
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsLiu J et al., "A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression.", Nat Commun, 2021 Sep 22;12(1):5578
SubmissionRegistration date: 24-Jun-2014
Equipe Radvanyi, UMR 144, Institut Curie
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes2230

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    Retinoblastoma genome methylation data
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