-
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Study
EGAS00001003018
-
Triple_Negative_Breast_Cancer_Whole_Genome_Validations
Study
EGAS00001000426
-
Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Study
EGAS00001003539
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Study
EGAS00001003053
-
Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma
Study
EGAS00001000622
-
HipSci Methylation analysis for embryonic stem cell control lines
Study
EGAS00001001728
-
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000551
-
Whole transcriptome RNA sequencing as comprehensive diagnostic tool for acute myeloid leukemia.
Study
EGAS00001003096
-
HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002023
-
Heritable pulmonary arterial hypertension in a large Iberian family
Study
EGAS00001003123
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
SLC9A3R1 variant associated with age-related hearing loss
Study
EGAS00001003072
-
Genomic profiling of paediatric glioma cell lines
Study
EGAS00001003006
-
A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
-
Histone acetylome-wide association study on tuberculosis infection
Study
EGAS00001003118
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Exome sequencing of advanced hepatocellular carcinoma
Study
EGAS00001003130
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003136
-
Whole exome sequencing of small cell neuroendocrine cancer of the cervix
Study
EGAS00001003142
-
DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
-
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Study
EGAS00001003063
-
Molecular Signature of Saudi Thyroid Cancer Using whole exome sequencing
Study
EGAS00001000680
-
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Study
EGAS00001000276
-
Breast_Cancer_Whole_Genome_Sequencing
Study
EGAS00001000210
-
A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy
Study
EGAS00001003177
-
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
-
Genome-wide association study of cervical cancer in East Asian populations
Study
EGAS00001003199
-
Triple_Negative_Breast_Cancer_RNA_Sequencing
Study
EGAS00001000377
-
Paroxysmal_neurological_Disorders
Study
EGAS00001000386
-
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Study
EGAS00001000392
-
FBSeq: RNA sequencing of human fetal brain.
Study
EGAS00001003214
-
Genomic profiling of esthesioneuroblastoma
Study
EGAS00001003225
-
BLUEPRINT Bisulfite-seq (CNAG)
Study
EGAS00001000418
-
Prostate_Cancer_Whole_Genome_Validations
Study
EGAS00001000427
-
Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Study
EGAS00001003248
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468
-
High_powered_complex_trait_association_mapping_through_whole_genome_sequencing_of_a_selected_subpopulation_of_the_INGI_Val_Borbera_genetic_isolate
Study
EGAS00001000398
-
Egypt_Genome_Project___high_coverage_whole_genome_sequencing
Study
EGAS00001000482
-
Transcriptional_profiling_of_tauopathies_in_human_IPS_derived_neurons
Study
EGAS00001000382
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Study
EGAS00001000492
-
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Study
EGAS00001003257
-
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
-
Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Study
EGAS00001000742
-
The subclonal architecture of metastatic breast cancer: Results from a prospective community-based rapid autopsy program 'CASCADE'
Study
EGAS00001002153
-
Autozygosity_pilot___British_Pakistani_from_Birmingham_2
Study
EGAS00001000567
-
Autozygosity_pilot_Born_in_Bradford
Study
EGAS00001000462
-
Autozygosity_pilot___Pakistani_from_Birmingham
Study
EGAS00001000511
-
MYD88/TLR mutations in CLL
Study
EGAS00001000772
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
Genetics_and_Networks_of_Congenital_Heart_Defects
Study
EGAS00001000762
-
High-resolution analyses of human sperm dynamic methylome reveals thousands of novel age-related epigenetic alterations
Study
EGAS00001004168
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
-
Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
-
Whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors
Study
EGAS00001000712
-
Detection of mutational patterns in cell free DNA (cfDNA) of colorectal cancer by custom amplicon sequencing
Study
EGAS00001003382
-
Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000687
-
Autozygosity_pilot___QMUL
Study
EGAS00001000717
-
Germline and somatic SMARCA4 mutations characterize small-cell carcinoma of the ovary, hypercalcemic type.
Study
EGAS00001000721
-
ESGI_Exome_sequencing_in_Circulating_Tumor_Cells_to_determine_therapy_related_markers_____
Study
EGAS00001000747
-
16S-based fecal microbiota composition of the Milieu Intérieur Cohort
Study
EGAS00001003419
-
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
-
The_Little_Princess_Knowledge_Bank_
Study
EGAS00001004237
-
Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma
Study
EGAS00001003438
-
Deciphering Developmental Disorders (DDD)
Study
EGAS00001000775
-
PSCP_bisulphite_analysis_in_hESCs
Study
EGAS00001001625
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
Exome sequencing of stroke cases with good or bad recovery three months after stroke
Study
EGAS00001003463
-
Integrative_genome_profiling_in_AML
Study
EGAS00001000858
-
HipSci HumanExome BeadChip analysis-Healthy volunteers
Study
EGAS00001000866
-
Chromatin 3D interactions mediate genetic effects on gene expression
Study
EGAS00001003485
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874
-
Molecular phenotyping of MCA/ID patients to improve diagnosis
Study
EGAS00001003489
-
HCA_Thymus_Disease
Study
EGAS00001004310
-
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Study
EGAS00001004326
-
Paroxysmal neurological disorders
Study
EGAS00001000048
-
Reconstituting the transcriptome and DNA methylome landscapes of human implantation at single-cell resolution
Study
EGAS00001003443
-
WTCCC3_Anorexia_Nervosa
Study
EGAS00001000913
-
METABRIC: Data from Batra et al (2021); DNA methylation landscapes of 1538 breast cancers reveal a replication-linked clock, epigenomic instability and cis-regulation
Study
EGAS00001004327
-
Dissecting intratumor heterogeneity of nodal B cell lymphoma on the transcriptional, genetic, and drug response level
Study
EGAS00001004335
-
Developmental_Dysplasia_of_the_Hip__DDH_
Study
EGAS00001000916
-
Genome_wide_association_study_of_vaccine_responses_in_infants_living_in_the_Developing_World__VaccGene___Phase_II_African_Cohorts
Study
EGAS00001000918
-
Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Study
EGAS00001004364
-
Whole-exome sequencing of extranodal NK/T cell lymphoma
Study
EGAS00001004357
-
Ischemic stroke in a Swedish case-control study.
Study
EGAS00001000936
-
Whole genome sequencing of 25 South African individuals with myasthenia gravis
Study
EGAS00001003462
-
Genome-wide prediction of human embryos
Study
EGAS00001001020
-
Genetic_profiling_of_mucosal_melanoma
Study
EGAS00001001115
-
DKFZ-HIPO Project H021/NCT MASTER
Study
EGAS00001000948
-
Genome-wide SNP genotyping and DNA methylation epigenotyping of African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001001066
-
Functional_characterisation_of_CpG_islands_in_human_and_mouse_tissues
Study
EGAS00001000075
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001003501
-
TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_
Study
EGAS00001000958
-
CRLF2_sequencing_project_Exomes
Study
EGAS00001000081
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Bone_Cancer___Rare_Types_Whole_Genome
Study
EGAS00001000501