{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"technology_type":["Illumina HiSeq 2000"],"study_type":["Cancer Genomics"],"full_dataset_link":["https://ega-archive.org/studies/EGAS00001000174"],"host":["EGA"],"description":["EGA study EGAS00001000174"],"dataset_title":["Balanced Ependymoma"],"repository":["EGA"],"category":["restricted"],"name_synonyms":["glioblastoma multiforme, Clear Cell Ependymoma, Anaplastic Ependymomas, oligodendroglioma, WHO grade II ependymal tumour, familial, astrocytoma, clear cell ependymoma (histologic variant), papillary ependymoma (histologic variant), subependymoma, benign, Anaplastic, Cellular Ependymoma, WHO grade II ependymal neoplasm, Papillary, Myxopapillary, Papillary Ependymoma, tanycytic ependymoma (histologic variant), Papillary., ependymoma, Ependymomas, Myxopapillary Ependymomas, Papillary Ependymomas, Myxopapillary Ependymoma, Anaplastic Ependymoma, glioma of brain, WHO grade II ependymal tumor, Ependymoma"],"description_synonyms":["Clear Cell Ependymoma, oligodendroglioma, glial cell tumor, \"malignant glioma - category\" EXACT [SNOMEDCT_2005_07_31:416500007], neuraxis, no ICD-O subtype\" EXACT [SNOMEDCT_2005_07_31:74532006], Central, WHO grade II ependymal tumour, malignant glioma, malignant, neoplasia, Neoplasms, neuroglial tumor, Cerebrospinal Axis, number, familial, clear cell ependymoma (histologic variant), neoplastic disease, Tumor, tumours, Anaplastic, Central Nervous Systems, NEOPL, Cerebrospinal, Central Nervous, Mutations, Myxopapillary, neoplastic growth, malignant Neuroglial tumor, Nervous Systems, heredity, Papillary Ependymoma, Systems, cerebrospinal axis, Myxopapillary Ependymomas, malignant\" EXACT [SNOMEDCT_2005_07_31:189909006], neoplasm, \"glioma, Neuroglial tumor, glioma of brain, WHO grade II ependymal tumor, Genomes., glioblastoma multiforme, Anaplastic Ependymomas, Nervous System, systema nervosum centrale, CNS, cell process disease, tumor disease, neoplasm (disease), neuroglial tumour, astrocytoma, tumour, papillary ependymoma (histologic variant), subependymoma, whole genome, benign, disease of cellular proliferation, Axis, Cellular Ependymoma, WHO grade II ependymal neoplasm, Papillary, \"malignant glioma (morphologic abnormality)\" EXACT [SNOMEDCT_2005_07_31:269505000], MALIGNANT AND UNSPECIFIED (INCL CYSTS AND POLYPS), \"malignant Neuroglial tumor\" EXACT [NCI2004_11_17:C4822], Cerebrospinal Axi, cardinality, tanycytic ependymoma (histologic variant), ependymoma, Ependymomas, Papillary Ependymomas, Axi, tumor, Myxopapillary Ependymoma, other neoplasm, glioma, Anaplastic Ependymoma, NEOPLASMS BENIGN, Neoplastic Growth, Neoplasia, Ependymoma, Tumors"],"additional_accession":[]},"is_claimable":false,"name":"Balanced Ependymoma","description":"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.","dates":{"updated":"2017-07-26 15:39:24"},"accession":"EGAS00001000174","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAD00001000350","EGAC00001000000"]}}