-
Genomic Epidemiology of Complex Diseases in Population-based Brazilian Cohorts
Study
EGAS00001001245
-
Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
-
Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
-
Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Study
EGAS00001001252
-
H3Africa - Trauma And Neurobiology: Maternal stress and transgenerational impact. Search for Epigenetic Markers
Study
EGAS00001006645
-
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
-
The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Study
EGAS00001001305
-
Genetic landscape of pediatric high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001001316
-
JMML targeted sequencing (2013)
Study
EGAS00001001324
-
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
-
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Study
EGAS00001001353
-
Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease
Study
EGAS00001004777
-
Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Study
EGAS00001001427
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
-
GENETIC HISTORY OF ITALY
Study
EGAS00001001458
-
T2D-GENES: Exome sequencing
Study
EGAS00001001460
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
-
Integrated genomic characterization of IDH1 mutant Glioma malignant progression
Study
EGAS00001001588
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Study
EGAS00001006865
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Study
EGAS00001006866
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Study
EGAS00001006881
-
Genetic history of the Comorian populations.
Study
EGAS00001002565
-
Genetic history of the Swahili population
Study
EGAS00001002569
-
Genetic landscape of ENKTCL
Study
EGAS00001006906
-
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Study
EGAS00001002597
-
The multifaceted genomic history of Ashaninka from Amazonian Peru
Study
EGAS00001006958
-
The_genetics_of_thinness_compared_to_obesity
Study
EGAS00001002624
-
H3Africa - Collaborative African Genomics Network
Study
EGAS00001002656
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
-
Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures.
Study
EGAS00001002684
-
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
-
cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort
Study
EGAS00001007059
-
Genetic_Overlap_between_Metabolic_and_Psychiatric_disease
Study
EGAS00001002723
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma
Study
EGAS00001002725
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001002742
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001002749
-
MeDALL epigenetics study
Study
EGAS00001002169
-
CD49f single-cell methylomes
Study
EGAS00001002789
-
Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas.
Study
EGAS00001002271
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS
Study
EGAS00001002858
-
Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES
Study
EGAS00001002863
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Study
EGAS00001002875
-
HipSci_RNASEQ_PID
Study
EGAS00001001990
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Study
EGAS00001003502
-
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Study
EGAS00001001501
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Study
EGAS00001003527
-
Renal_habitat_WXS
Study
EGAS00001003703
-
Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
-
Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
-
Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma
Study
EGAS00001004371
-
TULIPs decorate the three-dimensional genome of PFA ependymoma
Study
EGAS00001005476
-
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
-
Genetics of non-syndromic idiopathic autism spectrum disorders in India
Study
EGAS00001006060
-
Whole exome sequencing of germline DNA was performed and subsequent polymorphisms in genes known and putatively involved in the innate immune response to fungi were identified
Study
EGAS00001001542
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component)
Study
EGAS00001001558
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities
Study
EGAS00001006422
-
Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Study
EGAS00001001575
-
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
-
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
Data containing genome-wide SNP data from Northwestern Amazonia
Study
EGAS00001006767
-
Submission 36 - study_title 1
Study
EGAS50000000206
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
Genotype data from 'Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture.'
Study
EGAS00001006944
-
Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade
Study
EGAS00001007002
-
Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry
Study
EGAS00001007011
-
Submission 36 - study_title 2
Study
EGAS50000000207
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
EGAS00001007027
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Study
EGAS00001007045
-
Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis
Study
EGAS00001007057
-
Long-term organoid culture of a small intestinal neuroendocrine tumor
Study
EGAS00001007093
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts
Study
EGAS00001007111
-
Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse
Study
EGAS00001007128
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
Genetics of gene expression in primary human immune cells
Study
EGAS00000000109
-
Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Study
EGAS00000000115
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
Paroxysmal neurological disorders
Study
EGAS00001000048
-
Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
-
Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred
Study
EGAS00001000099
-
UK10K NEURO FSZ
Study
EGAS00001000118
-
UK10K NEURO ASD BIONED
Study
EGAS00001000111
-
UK10K NEURO ASD MGAS
Study
EGAS00001000113
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
UK10K NEURO IOP COLLIER
Study
EGAS00001000121
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
UK10K_RARE_HYPERCHOL
Study
EGAS00001000129