-
Acquisition_of_additional_mutations_drives_accelerated_progression_of_NPM1_positive_CMML_to_AML_
Study
EGAS00001000619
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Study
EGAS00001004380
-
AACR Project Genomics, Evidence, Neoplasia, Information, Exchange (GENIE)
Study
phs001337
-
IGNITE: Implementing GeNomics In practice: Genomic Medicine Implementation - The Personalized Medicine Program
Study
phs001978
-
Pediatric Preclinical Testing Consortium (PPTC)
Study
phs001437
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program - Neuroblastoma
Study
phs003163
-
Acquisition of additional mutations drives accelerated progression of NPM1 positive CMML to AML
Dataset
EGAD00001002194
-
Using NGS to Sequence Whole Genomes to Identify Genes Underlying ALS
Study
phs003067
-
Common origin and somatic mutation patterns of composite lymphomas and leukemias
Study
EGAS50000001017
-
Spatial and Temporal Homogeneity of Driver Mutations in Diffuse Intrinsic Pointine Glioma
Study
EGAS00001001654
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325
-
INCLUDE: Genetic Underpinnings of the Multifactorial Phenotype of Trisomy 21 Patients Unveiled by Multi-Omics Approaches
Study
phs002983
-
Altered enhancer-promoter interaction leads to MNX1 expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13)
Study
EGAS50000000130
-
The brain neurovascular epigenome and its association with dementia
Study
EGAS50000001160
-
Gene fusion and transcriptomic landscapes of sarcomas
Study
EGAS00001002189
-
Phylogenetic analysis of paired breast carcinomas identifies genetic events associated with clonal recurrence and invasive progression
Study
EGAS50000001298
-
Phenotypic characterization and prognostic impact of CD103+ tissue-resident memory T cells in diffuse large B cell lymphoma
Study
EGAS50000000943
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001585
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001598
-
RBMX functional retrocopy safeguards brain development
Study
EGAS50000001650
-
Aggressive genomic features in clinicallyindolent primary HHV8-negative effusion-based lymphoma
Study
EGAS00001002743
-
Enhancer profiling identifies epigenetic markers of endocrine resistance and reveals therapeutic options for metastatic castration-resistant prostate cancer patients (LuCaP cell line data)
Study
EGAS50000000917
-
Transcriptional_profiling_of_tauopathies_in_human_IPS_derived_neurons
Study
EGAS00001000382
-
cfDNA dataset from the urine supernatant of ovarian cancer patients and healthy controls
Study
EGAS00001007238