-
eQTL summary statistics
Dataset
EGAD00001005041
-
Whole Genome Sequencing data for epigenetic subgroups of meningioma
Dataset
EGAD00001005061
-
Somatic genetic basis of Wilms' tumour
Dataset
EGAD00001005134
-
Somatic genetic basis of Wilms' tumour
Dataset
EGAD00001005135
-
Somatic genetic basis of Wilms' tumour
Dataset
EGAD00001005136
-
The British Autozygosity Populations BioResource (2019-08-14)
Dataset
EGAD00001005253
-
ESGI - Whole Genome Sequencing of samples from the INGI-Val Borbera genetic isolate (X10) (2019-08-19)
Dataset
EGAD00001005268
-
DNA methylation and Metabolic data from type 2 diabetes adolescents
Dataset
EGAD00001005271
-
Phylogenetic development of childhood tumours
Dataset
EGAD00001005770
-
Somatic mutation and clonal evolution normal breast tissue TGS (2020-01-15)
Dataset
EGAD00001005787
-
Whole Genome Sequencing of Human Organoid Lines (2020-02-20)
Dataset
EGAD00001005995
-
Multiregional non-invasive genetic characterization of MM
Dataset
EGAD00001006028
-
Phylogenetic reconstruction of breast cancer
Dataset
EGAD00001006121
-
Analysis File for 87 Argentinean individuals
Dataset
EGAD00001006227
-
RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Dataset
EGAD00001006258
-
Epigenetic subtypes of neuroblastoma - ChIPseq
Dataset
EGAD00001006285
-
Epigenetic subtypes of neuroblastoma - RNAseq
Dataset
EGAD00001006286
-
Genomic and transcriptomic data of glioma specimens
Dataset
EGAD00001006299
-
The Transcriptional Landscape of SHH Medulloblastoma
Dataset
EGAD00001006305
-
Somatic mutations reveal embryonic genetic bottlenecks generating placental mosaicism
Dataset
EGAD00001006337
-
Pre-clinical evolution of haematological malignancies_WGS
Dataset
EGAD00001006423
-
Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial
Dataset
EGAD00001006585
-
Expression profiles and genetic makeup of agnospheres.
Dataset
EGAD00001006668
-
CINECA_synthetic_cohort_EUROPE_UK1 referencing fake samples
Dataset
EGAD00001006673
-
Whole Exome sequencing data from Shwachman-Diamond syndrome bone marrow samples
Dataset
EGAD00001006815
-
Dedifferentiated Melanoma (2021-02-02)
Dataset
EGAD00001006931
-
Fetal origins of malignant germ cell tumours
Dataset
EGAD00001007038
-
Genetic-epigenetic tissue mapping for plasma DNA: applications in prenatal testing, transplantation and oncology
Dataset
EGAD00001007041
-
HV31 - Illumina PCR-free sequencing
Dataset
EGAD00001007042
-
Targeted-capture sequencing (bam files) of 81 samples of myxofibrosarcoma and 44 matched pairs
Dataset
EGAD00001007826
-
Epigenetic profiles of neuroblastoma PDXs
Dataset
EGAD00001003394
-
GenomeDenmark Phase 2 - HLA validation sequencing data
Dataset
EGAD00001003454
-
Gene Characterization in Carbohydrate metabolic alterations (neonatel diabetes & congenital hyperinsulinemic) in early childhood (2018-03-14)
Dataset
EGAD00001004040
-
The contribution of POT1 variants to sporadic melanoma development (2018-06-06)
Dataset
EGAD00001004151
-
Genetic screening of GPI-anchor protein synthesis (2018-08-13)
Dataset
EGAD00001004294
-
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
-
RNAseq data of polyA+ RNA from Leukocytes from 624 individuals of the SardiNIA cohort.
Study
EGAS00001002105
-
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Study
EGAS00001002329
-
Whole genome bisulfite sequencing of hepatitis B virus-associated hepatocellular carcinoma tumor and non-cancerous samples
Study
EGAS00001002230
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Study
EGAS00001002594
-
Understanding_population_genetics_and_patterns_of_genome_wide_heterozygosity_in_a_sample_of_the_Croatian_isolated_populations__ESGIDalmatians_
Study
EGAS00001000336
-
CD49f single-cell methylomes
Study
EGAS00001002789
-
HER2_positive_Breast_Cancer_
Study
EGAS00001000042
-
The whole blood of female volunteers and sperm from the male volunteer were used to extract genomic DNA to do whole genome sequencing. Distinguished SNPs between parental genomes were retained to analyze parental allele-specific DNA methylation and chromatin accessibility in scCOOL-seq data.
Study
EGAS00001002987
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
Exome sequencing in bipolar disorder families
Study
EGAS00001003085
-
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
-
Histone acetylome-wide association study on tuberculosis infection
Study
EGAS00001003118
-
Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195
-
Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Study
EGAS00001003248
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
HG Transcriptome sequencing in the INTERVAL cohort
Study
EGAS00001003346
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
Whole genome shotgun sequencing and somatic mutations data in Hepatocellular carcinoma
Study
EGAS00001002578
-
Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy
Study
EGAS00001000460
-
Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
-
A_study_of_the_molecular_pathogenesis_of_Splenic_Marginal_Zone_and_Diffuse_Large_B_Cell_Lymphoma
Study
EGAS00001000335
-
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Study
EGAS00001002657
-
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
-
Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma
Study
EGAS00001002705
-
Resolving_the_Genetic_Architecture_of_Aseptic_Loosening_After_Total_Hip_Replacement
Study
EGAS00001001883
-
Human islet 3D chromatin maps provide insights into type 2 diabetes
Study
EGAS00001002917
-
Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML)
Study
EGAS00001002511
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
Study
EGAS00001000545
-
Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer
Study
EGAS00001000882
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer
Study
EGAS00001000682
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome
Study
EGAS00001002022
-
Genotyping_of_additional_Inflammatory_Bowel_Disease_cases___2014
Study
EGAS00001000924
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
Genetic history of the Swahili population
Study
EGAS00001002569
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
The Druze analysis group
Study
EGAS00001000963
-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
-
BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
-
HipSci Illumina 450K Methylation analysis-Rare_BBS
Study
EGAS00001001274
-
T2D-GENES: Exome sequencing
Study
EGAS00001001460
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
-
HipSci___Whole_Exome_sequencing___Kabuki
Study
EGAS00001001981
-
Genomic landscape of oral cancers (Illumina RNA-Seq)
Study
EGAS00001003237
-
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Study
EGAS00001001994
-
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
Genomic and Epigenomic Features of Primary and Recurrent Hepatocellular Carcinomas
Study
EGAS00001002094
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
-
Whole exome sequencing of Parkinson's disease patients from the United Kingdom
Study
EGAS00001002156
-
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Study
EGAS00001002597
-
The Ovarian Cancer Association Consortium OncoArray genome-wide association study
Study
EGAS00001002305
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001002749
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
HipSci___RNAseq___Rare_BBS
Study
EGAS00001001318