-
Single cell RNA sequencing of relapsed/refractory multiple myeloma
Study
EGAS00001004805
-
Mutagenic impact of radiotherapy in B-cell lymphoma and multiple myeloma
Study
EGAS50000000997
-
Comprehensive genetic landscape, immune checkpoint profiling, and establishment of patient-derived xenograft (PDX) of metachronous brain tumors from constitutive mismatch repair deficiency with a biallelic variant on MSH6
Study
EGAS50000000351
-
Methylome of medulloblastoma data (MB_COMICS cohort)
Study
EGAS00001007815
-
Drug Perturbation of Primary Lymphoma Patient Samples and RNA Sequencing
Study
EGAS50000001500
-
RNA-seq after drug perturbation of primary lymphoma samples
Dataset
EGAD50000002166
-
PTEN homozygous deletion is a negative prognostic factor in Tumor Treating Fields-treated glioblastoma, IDH wildtype patients
Study
EGAS50000001469
-
Targeted DNA sequencing of TTFields-treated glioblastoma, IDH wildtype
Dataset
EGAD50000002117
-
TTFields Glioblastoma Data Access Committee, Charité – Universitätsmedizin Berlin
Dac
EGAC50000000843
-
STimage: Robust and interpretable prediction of gene markers and cell types from spatial transcriptomics data
Dataset
EGAD50000002172
-
Rare Germline Variants in CDKN2A-Negative Children and Adolescents with Cutaneous Melanoma
Study
EGAS50000001311
-
Exome data from 154 patients with childhood or adolescent cutaneous melanoma
Dataset
EGAD50000001868
-
Tumor-reactive heterotypic CD8 T cell clusters from clinical samples
Study
EGAS50000000785
-
Visium CytAssist Spatial Gene Expression analysis for FFPE glioblastoma samples
Study
EGAS50000001242
-
3D chromatin analysis of clear cell renal cell carcinoma using micro-C
Study
EGAS50000001323
-
Chromatin accessibility of clear cell renal cell carcinoma
Study
EGAS50000001325
-
ChIP-seq analysis of clear cell renal cell carcinoma
Study
EGAS50000001322
-
Gene expression analysis of clear cell renal cell carcinoma
Study
EGAS50000001324
-
Recurrent COPA mutation drives R-spondin-independent Wnt activation in intestinal tumors
Study
JGAS000868
-
Non-small cell lung cancer molecular subtypes and vulnerability to immunotherapy treatment combinations
Study
EGAS50000001272
-
Contribution of specific cell types to the development of Barrett’s esophagus and carcinoma via germline genetic risk
Study
EGAS50000000530
-
RNAseq profile of monomorphic epitheliotropic intestinal T-cell lymphoma and enteropathy associated T-cell lymphoma
Study
EGAS50000001125
-
Whole Exome Sequencing of monomorphic epitheliotropic intestinal T-cell lymphoma and enteropathy associated T-cell lymphoma
Study
EGAS50000001126
-
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
-
CASCADE metastatic melanoma study
Study
EGAS00001004950
-
Chordoma_Sequencing_Project_Whole_Genome
Study
EGAS00001000409
-
Recurrent Somatic Mutations of PTPN1 in Primary Mediastinal B cell lymphoma and Hodgkin Lymphoma
Study
EGAS00001000554
-
ICGC Oesophageal adenocarcinoma - pilot samples
Study
EGAS00001000559
-
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
Osteosarcoma_RNAseq
Study
EGAS00001000615
-
Whole Genome sequencing of adult T-cell leukemia/lymphoma
Study
EGAS00001001210
-
Identification_of_drug_resistance_genes_in_melanoma
Study
EGAS00001000617
-
Transcriptome sequencing of hepatocellular carcinoma biopsies (proteogenomic study)
Study
EGAS00001005074
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Study
EGAS00001005243
-
Whole genome bisulfite sequencing of hepatitis B virus-associated hepatocellular carcinoma tumor and non-cancerous samples
Study
EGAS00001002230
-
Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma
Study
EGAS00001005314
-
Pediatric tumor in a single child of three large nuclear families
Study
EGAS00001005321
-
Burden_of_Disease_in_Sarcoma
Study
EGAS00001000087
-
Neuroblastoma tumor heterogeneity and cell plasticity (from patients)
Study
EGAS00001005322
-
UQCCR/QCMG brain metastasis sequence analysis
Study
EGAS00001000722
-
The mutational landscape of primary central nervous system lymphoma (Hipo H050, A050, XD013)
Study
EGAS00001005339
-
ICGC Oesophageal adenocarcinoma - lymph-node samples
Study
EGAS00001000727
-
Orphan_Tumour_Study___familial_neuroblastoma
Study
EGAS00001002171
-
Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Study
EGAS00001005395
-
Single-cell profiling maps the spectrum of crosstalk between glioma cells and tumor associated macrophages
Study
EGAS00001002185
-
Targeting the DNA Repair Pathway in Ewing Sarcoma
Study
EGAS00001000839
-
Genomic landscape of Ewing sarcoma (ICGC project)
Study
EGAS00001000855
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982