-
HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
-
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
-
Case Report: Precision medicine target revealed by in-vitro modelling of relapsed, refractory ALL from a child with neurofibromatosis
Study
EGAS00001006187
-
Time-dependent characterization of CNS response in COVID-19
Study
EGAS00001006442
-
Chip_seq_oesophageal_adenocarcinoma_
Study
EGAS00001007180
-
Transcriptomic analysis of cell-of-origin CNS neuroblastoma, FOXR2 activated
Study
EGAS00001007247
-
Single-cell RNA-seq of peripheral blood mononuclear cells in classic Hodgkin lymphoma
Study
EGAS00001007569
-
Integrated single-cell profiling dissects cell-state-specific enhancer landscapes of human tumor infiltrating T cells.
Dataset
EGAD00001008662
-
Duplexseq of the interstrand crosslinks_WGS
Dataset
EGAD00001010298
-
Whole genome sequencing of 198 epileptic individuals.
Dataset
EGAD00001004062
-
Submitter Portal
Documentation
submission/metadata/submission/sequencing-phenotype/submitter-portal
-
Molecular and Population Genetics (MPG) research at ICR DAC and POLA DAC
Dac
EGAC00001000328
-
DAC Liquid biopsies and matched tumor tissue - EwS and other pediatric sarcomas
Dac
EGAC00001002037
-
Mechanisms of Restoring T Cell Immunity after Cure of Chronic Viral Infection
Study
phs002510
-
Whole Genome Sequencing in the Inner City Asthma Consortium (ICAC) Cohorts
Study
phs002921
-
Genetic Analysis of Desmoplastic Melanoma
Study
phs000977
-
Functional Enhancer Elements Drive Subclass-Selective Expression From Mouse to Human Neocortex
Study
phs002292
-
Pediatric Investigation of Genetic Factors Linked with Renal Progression (PediGFR): Chronic Kidney Disease in Children Cohort (CKiD)
Study
phs000650
-
Genomic Analysis of Follicular Lymphoma
Study
phs002989
-
HudsonAlpha Long Read Sequencing Data of Individuals with Rare Suspected Genetic Conditions
Study
phs003537
-
Genetic Studies of Homologous Recombination Deficiency in Hispanic Gastric Cancer
Study
phs003251
-
Leukemia Relapse via Genetic Immune Escape after Allogeneic Hematopoietic Cell Transplantation
Study
phs003235
-
Whole Genome Sequencing for Metastatic Mutational Burden in Extraskeletal Myxoid Chondrosarcoma
Study
phs003305
-
A Therapeutic Vaccine for Fibrolamellar Hepatocellular Carcinoma
Study
phs003970
-
Investigation of molecular diagnosis by molecular biological analysis using next-generation sequencer for actionable endocrine diseases (including neoplastic diseases)
Study
JGAS000625
-
Ultra-Low-Pass Whole Genome Sequencing of Cell-Free DNA for Large B-Cell Lymphoma
Study
EGAS50000001027
-
Cambridge Neoadjuvant Cancer of the Prostate (CANCAP03): A Window Study into the Effects of Olaparib ± Degarelix in Primary Prostate Cancer.
Study
EGAS50000000880
-
E-cadherin inactivation shapes tumor microenvironment specificities in invasive lobular carcinoma
Study
EGAS50000001760
-
Transcriptomes of human CD4+ T lymphocytes - Metabolic project
Study
EGAS00001005565
-
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
-
Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
-
Gut microbiome modulates response to anti PD1 immunotherapy in metastatic melanoma patients
Study
EGAS00001002698
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
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
-
Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Study
EGAS00001003736
-
Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812
-
SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Study
EGAS00001002920
-
Targeted sequencing of diffuse large B-cell lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005953
-
Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Study
EGAS00001004786
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures
Study
EGAS00001006598
-
DNA methylation landscape of prostate cancer
Study
EGAS00001006670
-
Pre-activated anti-viral innate immunity in the upper airways controls early SARS-CoV-2 infection in children
Study
EGAS00001005461
-
The immunological characterization of expanded tumor-infiltrating lymphocytes in renal cell carcinoma patients
Study
EGAS00001006952
-
Type 1 Diabetes Genetics Consortium (T1DGC): Genome-Wide Association Study in Type 1 Diabetes, 2008
Study
phs000180
-
Copy-Number Analysis of Understudied Black Women Ovarian Cancers
Study
phs002313
-
Longitudinal Studies of Patients with Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)
Study
phs003075
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: TexGen
Study
phs003010
-
NHLBI TOPMed: Outcome Modifying Genes in Sickle Cell Disease (OMG)
Study
phs001608
-
Exceptional Responders Initiative
Study
phs001145
-
National Institute on Aging (NIA) SardiNIA Study
Study
phs000338
-
Kids First: Whole Genome Sequencing in Recessive Structural Brain Defects
Study
phs002590
-
Drug development for pediatric cancers: the importance of patient' s genomic data re-use
Blog
drug-development-for-pediatric-cancers
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
METABRIC
Study
EGAS00000000083
-
Genome_wide_association_study_of_vaccine_responses_in_infants_living_in_the_Developing_World__VaccGene___Phase_II_African_Cohorts
Study
EGAS00001000918
-
Base Editing Reduces Misfolded Protein Accumulation and Toxicity in Alpha-1 Antitrypsin Deficient Patient iPSC-Hepatocytes
Study
phs002471
-
The National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network (SiGN)
Study
phs000615
-
Systemic Inflammation and Lymphocyte Activation Precede Rheumatoid Arthritis
Study
phs003944
-
Genomic Copy-Number Variants Drive Apoptotic Resistance and Relapses on Immune Checkpoint Inhibitors
Study
phs004102
-
Development of the prevention and therapy of CRC using patient derived culture tissues.
Study
JGAS000139
-
Introducing Federated EGA Affiliates: a newly defined tier in the Federated EGA Network
Blog
fega-affiliates
-
RTEL1 mutation as a modifier of Dyskeratosis Congenita in a family with a Telomerase RNA (hTR) template mutation and variant telomeric repeats
Study
EGAS50000001644
-
Assessment of candidate high-grade serous ovarian carcinoma predisposition genes through integrated germline and tumour sequencing
Study
EGAS50000000770
-
Title: Divergent levels of CD112 and INKA1 define a distinct subset of human long-term hematopoietic stem cells
Dataset
EGAD00001006541
-
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
-
Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
-
reChIP-seq reveals widespread bivalency of H3K4me3 and H3K27me3 in CD4+ memory T-Cells
Study
EGAS00001001568
-
Interactions between the tumor and the systemic response of breast cancer patients
Study
EGAS00001001804
-
Whole genome, transcriptome and methylome profiling enhances actionable target discovery in high-risk paediatric cancer
Study
EGAS00001004572
-
Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
Study
EGAS00001004373
-
Single-cell Transcriptome Profiling of Treatment-naïve and Post-treatment Colorectal Cancer: Insights into Putative Mechanisms of Chemoresistance
Dac
EGAC50000000482
-
RNA-seq in LCLs derived from constitutional MLH1 epimutation carriers and non-carrier relatives
Study
EGAS50000000498
-
cell-free methylated DNA immunoprecipitation and high-throughput sequencing data for samples from liver transplant recpients with graft pathologies
Dataset
EGAD50000001727
-
Clinical and ctDNA data for IMpassion031
Dataset
EGAD50000001420
-
vaccgene_1000G_MKK_hla
Dataset
EGAD00010002577
-
Whole transcriptome and 850k methylome profiling of human MBM
Dataset
EGAD00001008508
-
Dataset for WES PCNSL
Dataset
EGAD00001010847
-
RNA-seq data from the tumor samples of head and neck cancer patients
Dataset
EGAD00001011279
-
Extensive and differential platinum chemotherapy mutagenesis in livers of children - Whole genome NanoSeq
Dataset
EGAD00001016142
-
Whole genome sequencing and whole exome sequencing of pediatric osteosarcoma
Dataset
EGAD00001004482
-
Women's Health Study Accelerometry Dataset
Study
phs001964
-
Assessment of Health-related Quality of Life in Rare Kidney Stones
Study
phs001770
-
Genetic Analysis of the Chiari I Malformation
Study
phs001795
-
National Eye Institute (NEI) Age-Related Eye Disease Study 2 (AREDS2)
Study
phs002015
-
Metagenomic Analysis to Identify Novel Infectious Agents in Systemic Anaplastic Large Cell Lymphoma
Study
phs002064
-
Bone Microarchitecture
Study
phs002102
-
Genetic defects in familial renal disorders
Study
phs000477
-
National Institute on Aging - Late Onset Alzheimer's Disease Family Study: Genome-Wide Association Study for Susceptibility Loci
Study
phs000168
-
Foundation Medicine Adult Cancer Clinical Dataset (FM-AD)
Study
phs001179
-
ARDSnet and the iSPAAR Consortium: Genomic Basis of Susceptibility and Outcomes in Patients with the Acute Respiratory Distress Syndrome (ARDS)
Study
phs000631
-
A prospective study identifies MisMatch Repair genes as candidate predisposing genes for uveal melanoma.
Study
EGAS50000000914
-
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
-
Genome-wide DNA methylation sequencing identifies epigenetic perturbations in the upper airways under long-term exposure to moderate levels of ambient air pollution
Study
EGAS00001007374
-
Successful immune checkpoint blockade in a patient with advanced stage microsatellite unstable biliary tract cancer (H021)
Study
EGAS00001002441
-
HDAC3 mediates the inflammatory response and LPS tolerance in human monocytes and macrophages
Study
EGAS00001004218
-
Obesity and hyperinsulinemia drive adipocytes to activate a cell cycle program and senesce
Study
EGAS00001005770
-
GSCAN GWAS Meta-analysis of Tobacco and Alcohol use (GSCAN-GWAS)
Study
phs001809
-
NHLBI TOPMed: Study of African Americans, Asthma, Genes and Environment (SAGE)
Study
phs000921
-
Merkel Cell Carcinoma Tissue and Data Repository
Study
phs002189