-
Genomic Landscape and Clonal Architecture in Pediatric Myeloid Neoplasms with Chromosome 7 Deletions
Study
EGAS00001008055
-
Whole Genome Sequencing of Liver Cancers
Study
EGAS00001002408
-
Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells
Study
EGAS00001001234
-
Molecular sub-classification of hormone receptor-positive breast cancer
Study
EGAS00001004594
-
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Study
EGAS00001005243
-
Profiling_heterogeneity_in_Human_derived_IPSC_neurons
Study
EGAS00001002885
-
RP-1843 Arcagen - Gastrointestinal rare cancers (GI)
Study
EGAS00001006299
-
Profiling of childhood neuroblastoma and the immune microenvironment by single-cell sequencing of RNA and TCR
Study
EGAS00001006823
-
Clonally resolved single-cell multi-omics identifies routes of cellular differentiation in acute myeloid leukemia
Study
EGAS00001007078
-
Characterization of genomic landscape of Peripheral T-cell Lymphomas, not otherwise specified (PTCL-NOS) (2018-10-30)
Dataset
EGAD00001004428
-
EGA synthetic data
Documentation
synthetic-data
-
Transcriptomic profiling of circulating regulatory T cells from follicular lymphoma patients before and after Lenalidomide treatment
Study
EGAS50000001048
-
SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
-
Childhood Cancer Survivor Study (CCSS)
Study
phs001327
-
NCI Expanded Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs001736
-
Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)
Study
phs000652
-
Multicenter Study of Hydroxyurea (MSH)
Study
phs002348
-
NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)
Study
phs001467
-
Whole Genome Association Study of Systemic Lupus Erythematosus
Study
phs000122
-
Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
-
Japan PBC-GWAS Haplotype Study
Study
EGAS00001002915
-
Transcriptomic analysis of peripheral blood dendritic cells and monocytes from patients with familial chilblain lupus and hetereozygous mutations in TREX1
Study
EGAS00001006215
-
SNPArray_Thai
Dataset
EGAD00010002285
-
Redefined indel taxonomy reveals insights into mutational signatures
Dataset
EGAD50000000209
-
Servicio Hematología_Hospital Universitario de Salamanca_Spain
Dac
EGAC50000000155