-
Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Genomic profiling of esthesioneuroblastoma
Study
EGAS00001003225
-
High-resolution analyses of human sperm dynamic methylome reveals thousands of novel age-related epigenetic alterations
Study
EGAS00001004168
-
Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001004192
-
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Study
EGAS00001003063
-
Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
-
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
-
The_Little_Princess_Knowledge_Bank_
Study
EGAS00001004237
-
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
-
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
-
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
-
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Study
EGAS00001004326
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Study
EGAS00001000416
-
BLUEPRINT Bisulfite-seq (CNAG)
Study
EGAS00001000418
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Prostate_Cancer_Whole_Genome_Validations
Study
EGAS00001000427
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468
-
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
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
High_powered_complex_trait_association_mapping_through_whole_genome_sequencing_of_a_selected_subpopulation_of_the_INGI_Val_Borbera_genetic_isolate
Study
EGAS00001000398
-
Uterine leiomyoma: DNA methylation, chromatin activity and gene expression
Study
EGAS00001004499
-
Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Study
EGAS00001000742
-
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
-
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
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552
-
MYD88/TLR mutations in CLL
Study
EGAS00001000772
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
A GWAS for cutaneous leishmaniasis in Brazil
Study
EGAS00001004596
-
Detection of mutational patterns in cell free DNA (cfDNA) of colorectal cancer by custom amplicon sequencing
Study
EGAS00001003382
-
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
-
Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000687
-
16S-based fecal microbiota composition of the Milieu Intérieur Cohort
Study
EGAS00001003419
-
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
-
Prognostic and therapeutic significance of leukemia subtypes and minimal residual disease measurements in pediatric acute lymphoblastic leukemia treated with contemporary risk-directed trial: a cohort study
Study
EGAS00001004739
-
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
-
Dataset with genome-wide array data from Algerian Amazigh (Chaoui and Mozabite) and non-Amazigh individuals
Study
EGAS00001007235
-
Genetics_and_Networks_of_Congenital_Heart_Defects
Study
EGAS00001000762
-
Deciphering Developmental Disorders (DDD)
Study
EGAS00001000775
-
Methylation analysis for plasma DNA of patients with organ transplantation
Study
EGAS00001004788
-
PSCP_bisulphite_analysis_in_hESCs
Study
EGAS00001001625
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
Integrative_genome_profiling_in_AML
Study
EGAS00001000858
-
HipSci HumanExome BeadChip analysis-Healthy volunteers
Study
EGAS00001000866
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874
-
Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
-
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
-
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
-
Genome-wide prediction of human embryos
Study
EGAS00001001020
-
Ischemic stroke in a Swedish case-control study.
Study
EGAS00001000936
-
Whole genome sequencing of 25 South African individuals with myasthenia gravis
Study
EGAS00001003462
-
DKFZ-HIPO Project H021/NCT MASTER
Study
EGAS00001000948
-
Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
-
Genetic_profiling_of_mucosal_melanoma
Study
EGAS00001001115
-
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
-
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
-
Exome and transcriptome sequencing of Desmoplastic Small Round Cell Sarcoma
Study
EGAS00001004575
-
Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
-
Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets
Study
EGAS00001001002
-
MDS Sequencing Project_Cancer Cell
Study
EGAS00001001011
-
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Study
EGAS00001001012
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
Dilgom_Exome
Study
EGAS00001000086
-
Whole genome sequencing of ASD quartet families
Study
EGAS00001001023
-
Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Study
EGAS00001000667
-
Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
-
The Genetic History of Greenlandic-European contact
Study
EGAS00001004933
-
Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders
Study
EGAS00001004949
-
ESGI___Whole_Genome_Sequencing_of_samples_from_the_INGI_Val_Borbera_genetic_isolate__X10_
Study
EGAS00001001123
-
Congenital_anosmia_1
Study
EGAS00001001124
-
Genome-wide association analysis on five isolated populations - Erasmus Rucphen Family (ERF) Study
Study
EGAS00001001134
-
HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Study
EGAS00001003519
-
Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants
Study
EGAS00001003521
-
Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Study
EGAS00001001174
-
Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Study
EGAS00001001182
-
Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191