-
The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH
Study
EGAS00001004285
-
Targeted_sequencing_of_embryonic_variants___Warm_Autopsy
Study
EGAS00001003952
-
Molecular classification improves risk assessment in adult B-lineage ALL: Patients on the international UKALLXII-ECOG2993 trial.
Study
EGAS00001004638
-
Whole genome sequencing of EBV Associated Nasopharyngeal Carcinoma
Study
EGAS00001004705
-
Single Cell ATAC-Seq on human cord-blood derived HSPC.
Study
EGAS00001004740
-
Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
-
Genomic_characterisation_of_MGUS__
Study
EGAS00001004124
-
Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021)
Study
EGAS00001004277
-
Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Study
EGAS00001004289
-
Prime editing for functional repair in patient-derived disease models
Study
EGAS00001004611
-
Bulk ATAC-Seq on sorted cord blood hematopoietic populations
Study
EGAS00001004742
-
Targeting AXL Kinase Uniquely Sensitizes Therapy-Insensitive Leukemic Stem and Progenitor Cells to Venetoclax Treatment in Acute Myeloid Leukemia
Study
EGAS00001004663
-
Hi-C on the OCIAML-2 Cell Line
Study
EGAS00001004743
-
Low-C on Human CB-derived LT-HSC and ST-HSC
Study
EGAS00001004744
-
ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line
Study
EGAS00001004741
-
Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Study
EGAS00001004786
-
Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma
Study
EGAS00001004371
-
Non-coding mutations reveal cancer driver cistromes in luminal breast cancer
Study
EGAS00001005235
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
Adult-type Granulosa Cell Tumour of the Ovary
Study
EGAS00001005414
-
Characterization of DLBCL with a PMBL gene expression signature
Study
EGAS00001005057
-
Sensitive and reproducible cell-free methylome quantification with synthetic spike-in controls
Study
EGAS00001005069
-
Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity
Study
EGAS00001005227
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Study
EGAS00001005405
-
Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021)
Study
EGAS00001005537
-
WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
-
Defining structural variation associated with breast cancer susceptibility by long-read genome sequencing
Study
EGAS00001005872
-
Multi-omic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target
Study
EGAS00001005647
-
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Study
EGAS00001006870
-
Multi-organ landscape of therapy-resistant melanoma
Study
EGAS00001006644
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Study
EGAS00001006904
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
Neuroblastoma Evolution
Study
EGAS00001006533
-
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures (Hipo_021)
Study
EGAS00001006629
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Study
EGAS00001006865
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Study
EGAS00001006866
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Study
EGAS00001006881
-
Data containing genome-wide SNP data from Northwestern Amazonia
Study
EGAS00001006767
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities
Study
EGAS00001006422
-
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
Genotype data from 'Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture.'
Study
EGAS00001006944
-
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
Genetic immune escape landscape in primary and metastatic cancer
Study
EGAS00001006123
-
Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis
Study
EGAS00001007057
-
Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation.
Study
EGAS00001007115
-
TULIPs decorate the three-dimensional genome of PFA ependymoma
Study
EGAS00001005476
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
-
International Multiple Sclerosis Genetics (IMSGC) Data Access Committee
Dac
EGAC00001001662