-
Evolution of a FLT3-TKD mutated subclone at meningeal relapse in acute promyelocytic leukemia (H021)
Study
EGAS00001001848
-
Healthy_ageing_thymus
Study
EGAS00001004311
-
Exome-wide mutation analysis of cell-free DNA to simultaneously monitor the full spectrum of cancer treatment outcomes
Study
EGAS00001005906
-
Transcriptome Sequencing PPGL
Study
EGAS00001006044
-
Butyrate producers as potential next-generation probiotics: safety assessment of the administration of Butyricicoccus pullicaecorum to healthy volunteers
Study
EGAS00001003276
-
Non-viral precision T cell receptor replacement for personalized cell therapy
Study
EGAS00001006898
-
Peripheral blood DNA methylome in adalimumab-treated patients with rheumatoid arthritis
Study
EGAS00001007578
-
ETMR_Meth
Dataset
EGAD00010001669
-
Prediction of plasma ctDNA fraction and prognostic implications of liquid biopsy in advanced prostate cancer
Dataset
EGAD50000000303
-
Somatic Mutations in Variant and IGHV4-34 Expressing Hairy Cell Leukemia
Study
phs000671
-
Tumor heterogeneity and acquired drug resistance in FGFR2 fusion-positive cholangiocarcinoma through rapid research autopsy
Study
phs001830
-
Clinical and molecular features of early onset pancreatic cancer
Study
EGAS50000000362
-
Autosomal dominant macular dystrophy associated with THRB: identification of new families and variants 
Study
EGAS50000000861
-
scRNAseq dataset of circulating T cells in FL patient before and after Lenalidomide treatment
Dataset
EGAD50000001529
-
NICOLA QUB Genetic
Dataset
EGAD00010002762
-
Single-cell genotype-to-phenotype mapping via co-capture of DNA mutations and mRNA transcripts
Dac
EGAC50000000833
-
WGS data of paediatric B-other B cell acute lymphoblastic leukemia (set6)
Dataset
EGAD50000002161
-
PDAC clinical phenotype data with CA19-9 and Lewis antigen status
Dataset
EGAD50000002254
-
Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)
Study
EGAS00001003662
-
SCLC CTC genomic analysis data set
Dataset
EGAD00001002678
-
Whole genome sequencing of Cas9 repaired cystic fibrosis organoids description
Dataset
EGAD00001005427
-
Low-pass whole-genome DNA sequencing of cohesin-mutated and wildtype adult AMLs
Dataset
EGAD00001011207
-
WES data of primary tumors and metastasis corresponding to three patients
Dataset
EGAD00001010173
-
Shallow whole genome sequencing from plasma DNA of BC, CRC and NSCLC patients
Dataset
EGAD00001006288
-
Combined single cell immunophenotyping and genotyping of adult low hypodiploid acute lymphoblastic leukemia
Dataset
EGAD00001009763
-
subset of 11 samples RRMM (RNA-Seq and WGS) from study EGAS00001005973 used also in study EGAS00001006538
Dataset
EGAD00001009679
-
Single Cell Transcriptomics of peripheral immune cells pre- and post-Immune Checkpoint Blockade
Dataset
EGAD00001007942
-
4C-seq in endometrial healthy and tumor tissues
Dataset
EGAD00001010897
-
cfDNA methylation profiling in Metastatic Cancer and Cancer of Unknown Primary
Dataset
EGAD00001011178
-
Mapping of runs back to samples for snRNASeq data
Dataset
EGAD00001015609
-
Alopecia and Vitiligo
Dataset
EGAD00001005289
-
Copy number profiling of tissue and plasma samples from high grade serous epithelial ovarian cancer patients
Dataset
EGAD00001006422
-
Delineate genomic and epigenomic changes in esophageal squamous cell carcinoma following radiotherapy
Dataset
EGAD00001003799
-
Genomic (WGS) data for the validation of the glioblastoma progression study (GBMatch).
Dataset
EGAD00001004077
-
Whole genome sequencing of 40 gastric cancer tumours and matched normal samples from Singapore.
Dataset
EGAD00001004279
-
Transcriptome (RNA-seq) data for the validation of the glioblastoma progression study (GBMatch).
Dataset
EGAD00001004076
-
Edinburgh Naevi Cohort (2018-08-03)
Dataset
EGAD00001004273
-
GIS-LUNGTCR1-2016_WES-FASTQ
Dataset
EGAD00001001978
-
Exome data: Histone mutations in human Pre-Leukemic HSC and AML
Dataset
EGAD00001004436
-
Whole Exome (WE) sequencing data files for H_NO-JB001
Dataset
EGAD00001001252
-
Whole genome sequencing data from whole genome amplified single cells and unamplified bulk samples
Dataset
EGAD00001004195
-
The Transcriptome of PLX4032 resistance
Dataset
EGAD00001000599
-
Ulcerative Colitis Human Microbiome Project (UCHMP)
Study
phs000262
-
A New Reference Panel to Boost African American Genotype Imputation
Study
phs001798
-
National Eye Institute (NEI) Ocular Hypertension Treatment Study (OHTS)
Study
phs000240
-
NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for Studying the Impact of Genetic Variation on Molecular Phenotypes
Study
phs000924
-
Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
-
INCLUDE: The Epidemiology of Transient Leukemia in Newborns with Down Syndrome
Study
phs002982
-
Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT-BioLINCC)
Study
phs003654
-
Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C)
Study
phs000430
-
Data access committee (DAC) in the Graduate School of Medical Science and Engineering (GSMSE) at Korea Advanced Institute of Science and Technology (KAIST)
Dac
EGAC00001001643
-
DAC of The polarity and specificity of antiviral T lymphocyte responses determine susceptibility to SARS-CoV-2 infection in cancer patients and healthy individuals
Dac
EGAC00001002517
-
Gastric and Esophageal tumour rearrangement screen
Dataset
EGAD00001000075
-
Circulating tumor DNA, pathological and immunologic responses to neoadjuvant nivolumab or nivolumab plus relatlimab and chemoradiotherapy in resectable esophageal/gastroesophageal junction cancer
Study
EGAS00001007299
-
WES in Angolan and Cape Verdean triple-negative breast cancer samples
Dac
EGAC50000000486
-
Ovarian subtypes tumor methylation data
Dataset
EGAD00010002773
-
endogene.bio
Dac
EGAC50000000786
-
Breast_Heterogeneity_Validation
Study
EGAS00001001972
-
Nasal brushes analysis
Study
EGAS00001006657
-
Metadata file
Dataset
EGAD00001008792
-
A New Pipeline to Predict and Confirm Tumor Neoantigens Predicts Better Response to Checkpoint Blockade
Study
phs002269
-
Cell Type-Specific and Disease-Associated eQTL in the Human Lung
Study
phs003521
-
Evaluation Study of Congestive Heart Failure and Pulmonary Artery Catheterization Effectiveness (ESCAPE-BioLINCC)
Study
phs003782
-
Biopsy-Derived Organoids in Personalised Early Breast Cancer Care: Challenges of Tumour Purity and Normal Cell Overgrowth Cap Their Practical Utility
Study
EGAS50000000605
-
Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Study
EGAS00001003661
-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
NIPT samples for systematic evaluation of BinDel, a software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Dataset
EGAD00001009512
-
Colon cancer targeted sequencing study contaning WBCs, primary tumor tissue and plasma samples
Study
EGAS50000000059
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000160
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000162
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000158
-
Karyotype Evolution in Response to Chemoradiotherapy and Upon Recurrence of Esophageal Adenocarcinomas
Study
EGAS00001007711
-
Improved detection of colibactin-induced mutations by genotoxic E. coli in organoids and colorectal cancer
Study
EGAS50000000212
-
Genetic Determinants of EGFR-Driven Lung Cancer Growth and Therapeutic Response In Vivo
Study
phs002334
-
Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia
Study
phs001372
-
Mitochondrial Abnormalities in Schizophrenia and Bipolar Disorder
Study
phs002395
-
Interpreting molecular role of DNA variants associated with Crohn's Disease through integrative analysis of open chromatin, epigenome and transcriptome data in diverse and relevant tissues and cells
Study
phs001418
-
Genomic Analysis of Paired Endometrial Cancer Primaries and Metastases
Study
phs001127
-
Structurally Complex Osteosarcoma Genomes Exhibit Limited Heterogeneity within Individual Tumors and across Evolutionary Time
Study
phs003209
-
L1-Seq and Genome-Wide SNP Genotyping in a Multiethnic Asian Population
Study
phs000732
-
Integrative Age-Related Changes in Genome and Epigenome in Human Lung in Relation to Smoking
Study
phs003317
-
Spatial Transcriptomics Reveals Discrete Tumor Microenvironments and Autocrine Loops Within Ovarian Cancer Subclones
Study
phs003561
-
Structure of the Mucosal and Stool Microbiome in Lynch Syndrome
Study
phs002343
-
Plasma mutation profile of precursor lesions and colorectal cancer using the Oncomine Colon cfDNA Assay
Study
EGAS50000000471
-
A single-chain derivative of the integrin β1-activating TS2/16 antibody potentiates organoid growth in Matrigel and Collagen hydrogels.
Study
EGAS50000001113
-
Single cell RNA sequencing of human embryonic forebrain after slice culturing for between four weeks and one month
Study
EGAS50000001185
-
Data Use Ontology (DUO) at EGA
Blog
data-use-ontology
-
Single cell transcriptomic analysis of the immune cell compartment in the human small intestine and in Celiac disease
Study
EGAS00001003751
-
White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer
Study
EGAS00001004114
-
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
-
Improving CLL Vγ9Vδ2-T cell fitness for cellular therapy by ex vivo activation and ibrutinib
Study
EGAS00001003193
-
Familial adult myoclonic epilepsy in Sri Lankan and Indian families
Study
EGAS00001004012
-
Resolving the immune landscape of human prostate at a single cell level in health and cancer
Study
EGAS00001005787
-
Transcriptional profiling of tauopathies in human IPS-derived neurons (2019-08-21)
Dataset
EGAD00001005277
-
RaScALL: Rapid (Ra) screening (Sc) of RNA-seq data for prognostically significant genomic alterations in acute lymphoblastic leukaemia (ALL)
Dataset
EGAD00001009087
-
Motif-directed chromatin repression by BCL11B shapes ectopic targeting and lineage commitment
Study
EGAS50000001719
-
Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening
Study
phs001482
-
Clinical and genetic analysis of retinopathy of prematurity - GWAS
Study
phs002020
-
HiDEF-seq single-molecule sequencing of single-strand mismatches and damage
Study
EGAS50000000318
-
Comparison of WGBS, EPIC array, EM-seq, and Nanopore sequencing in assessing DNA methylation marks
Study
EGAS00001008014