-
Dataset that contains runs of submission 12
Dataset
EGAD50000000040
-
Dataset that contains runs of submission 14
Dataset
EGAD50000000044
-
Genetic scoring guide for personalized risk assessment in pediatric B-cell precursor Acute Lymphoblastic Leukemia
Study
EGAS00001007239
-
Dataset that contains runs of submission 19
Dataset
EGAD50000000086
-
Genetic architecture of autism spectrum disorder in India
Dataset
EGAD00001008621
-
Dataset that contains runs of submission 15
Dataset
EGAD50000000082
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006233
-
Capturing sex-specific and infertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome
Study
EGAS00001006643
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort
Study
EGAS00001007059
-
Single-cell study of 14 childhood medulloblastoma patients
Dataset
EGAD00001009057
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - WGS
Dataset
EGAD00001010872
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - TGS
Dataset
EGAD00001010874
-
Dataset that contains runs of submission 27
Dataset
EGAD50000000112
-
Novel mutations in TOP2A in gliomas
Study
EGAS00001004556
-
Genomic and transcriptomic data of glioma specimens
Dataset
EGAD00001006299
-
Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade
Study
EGAS00001007002
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
Submission 84 - study_title 1
Study
EGAS50000000120
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010913
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010914
-
Cologne University Hospital, Institute of Human Genetics, Pathomechanisms of Rare Kidney Diseases Research Group DAC
Dac
EGAC00001003295
-
GDAP - Genome Diversity in Africa Project (2021-02-12)
Dataset
EGAD00001006965
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Dataset
EGAD00001011067
-
Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
-
Influence of the Microbiome on Epigenetic Mechanisms in IBD
Dataset
EGAD00001011066
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Dataset
EGAD00001011260
-
Cancer Genetics Data Access Commitee
Dac
EGAC00001001742
-
Longitudinal RNA-seq datasets from patients after abdominal surgery
Dataset
EGAD00001011102
-
Genetics of gene expression in primary human immune cells Data Access Committee
Dac
EGAC00001003318
-
Genetics of gene expression in primary human immune cells Data Access Committee
Dac
EGAC00001003327
-
Enhancer-gene rewiring in the pathogenesis of Quebec Platelet Disorder
Study
EGAS00001004315
-
The Haemgen RBC study
Study
EGAS00000000132
-
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts
Study
EGAS00000000056
-
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Study
EGAS00001000053
-
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Study
EGAS00001002517
-
Local In Time Statistics for processual research
Study
EGAS00001002520
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
Kibbutzim Family study
Study
EGAS00001002782
-
Molecular analysis of giant cell lesions
Study
EGAS00001002910
-
BLUEPRINT DNase accessibility (NCMLS)
Study
EGAS00001000351
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
Whole-exome sequencing of acute erythroid leukemia
Study
EGAS00001003696
-
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Study
EGAS00001000719
-
Genomic diversity of the African-descent Makranis of Pakistan
Study
EGAS00001002558
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Study
EGAS00001003159
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Study
EGAS00001001184
-
Human Genetics 5, Genome Institute of Singapore.
Dac
EGAC00001000412
-
The Druze analysis group
Study
EGAS00001000963