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Adeno-associated virus in the liver: natural history and consequences in tumor development
Study
EGAS00001003310
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Single cell multi-omics analysis of chromothriptic medulloblastoma highlights genomic and transcriptomic consequences of genome instability
Study
EGAS00001005410
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Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
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Single-cell RNA-seq of peripheral blood mononuclear cells in classic Hodgkin lymphoma
Study
EGAS00001007569
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Germline variants in patients diagnosed with both uveal and cutaneous melanoma
Study
EGAS00001007584
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Transcriptomic analysis of cell-of-origin CNS neuroblastoma, FOXR2 activated
Study
EGAS00001007247
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RNA-seq, WGS and WES of Hepatocellular carcinomas, enriched in fibrolamellar carcinomas
Study
EGAS00001003837
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Translation of non-canonical open reading frames as a cancer cell survival mechanism in childhood medulloblastoma
Study
EGAS00001007426
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Chromatin landscape of medulloblastoma reveals context dependent driver
Study
EGAS00001006741
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Alternative splicing in Shh-MB
Study
EGAS00001003220
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The impact of mutational clonality in predicting the response to anti-PD-L1/PD-L1 in advanced urothelial cancer
Study
EGAS00001007086
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Serial TERT rearrangement breakpoint quantification in circulating tumor DNA enables minimal residual disease monitoring in patients with neuroblastoma
Study
EGAS00001007365
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ICGC Oesophageal adenocarcinoma - Barrett's samples
Study
EGAS00001000726
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MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
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Discriminating Th17.1 cell driven sarcoidosis-like inflammation from relapse after anti-BCMA CAR T cells in multiple myeloma
Study
EGAS00001006133
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Intellance-2: omics data on recurrent glioblastoma patients participating in the Intellance-2 clinical trial, prior to treatment.
Study
EGAS00001005437
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Xenograft_Sequencing
Study
EGAS00001000140
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Bolleboom-Gao peri-tumoral snRNA-seq glioblastoma dataset 2022/A
Study
EGAS00001006935
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Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes
Study
EGAS00001004235
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Copy-number signatures and mutational processes in ovarian carcinoma
Study
EGAS00001002557
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Exploring high-throughput drug sensitivity testing in neuroblastoma cell lines and patient-derived tumor organoids in the era of precision medicine
Study
EGAS00001007160
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OAC WGS
Study
EGAS00001006470
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Monocyte Spike-in RNASeq
Study
EGAS00001007197
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Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
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Array-based methylation analysis of SDHB-deficient pheochromocytoma and paraganglioma
Study
EGAS00001007844