-
Y_phylogeny_haplogroupDE
Study
EGAS00001002674
-
ADCC_Exome_Sequencing
Study
EGAS00001000193
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001002749
-
Whole_exome_sequencing_of_rare_autoimmune_related_phenotypes
Study
EGAS00001000228
-
Osteosarcoma_Exome_Sequencing
Study
EGAS00001000163
-
Exome sequencing of 142 gastric cancer and matched normal from Japanese cohorts (UT)
Study
EGAS00001002891
-
SPATC1L variants associated with age-related and hereditary hearing loss
Study
EGAS00001003047
-
Triple_Negative_Breast_Cancer_Whole_Genome_Validations
Study
EGAS00001000426
-
Whole exome DNA sequence profiling of spatial biopsies of high grade serous epithelial ovarian cancer
Study
EGAS00001003048
-
Osteosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000278
-
Meningioma_Targeted_Sequencing_Study
Study
EGAS00001000282
-
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
-
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M-mutant pediatric high-grade gliomas
Study
EGAS00001000578
-
Whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors
Study
EGAS00001000712
-
Mutation tracking in single cell RNA-Seq reveals consequences of subclonal evolution in acute myeloid leukemia
Study
EGAS00001003414
-
16S-based fecal microbiota composition of the Milieu Intérieur Cohort
Study
EGAS00001003419
-
Spinocerebellar ataxia type 3 RNA-sequencing study
Study
EGAS00001004241
-
Exome sequencing of stroke cases with good or bad recovery three months after stroke
Study
EGAS00001003463
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001003501
-
300-Obese: clinical cohort of obese individuals, Nijmegen, the Netherlands
Study
EGAS00001003508
-
2014 chunnam AML analysis
Study
EGAS00001001082
-
International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results
Study
EGAS00001005110
-
Exome sequencing of patients with rare neurological disorders
Study
EGAS00001000159
-
DIPG RNA and exome sequencing
Study
EGAS00001004749
-
Gene expression profile of mesothelial-derived carcinoma-associated fibroblasts
Study
EGAS00001003747