-
Transcriptome profiling of three giant cell tumour of bone cell lines
Study
EGAS00001006441
-
Endothelium-derived stromal cells contribute to bone marrow niche formation
Study
EGAS00001004946
-
Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma
Study
EGAS00001004371
-
Tumorigenic role of Musashi-2 in aggressive mantle cell lymphoma
Study
EGAS00001006613
-
Single cell RNAseq of lung adenocarcinoma
Study
EGAS00001005021
-
Identification of genomic aberrations in low-grade serous ovarian cancer
Study
EGAS00001006679
-
Tissue DNA, WBC DNA and cfDNA (deep-)sequencing of mCRC patients treated with doublet chemotherapy and anti-EGFR in the CAIRO5 study
Study
EGAS00001006695
-
Whole Genome Sequencing Data of High Grade Serous Ovarian Cancer
Study
EGAS00001006775
-
Cachexia - Non-Cachexia Metagenome Analysis
Study
EGAS00001007156
-
Multiomic profiling of pleomorphic rhabdomyosarcoma
Study
EGAS00001007230
-
Comprehensive single-cell genome analysis at nucleotide resolution using the PTA Analysis Toolbox
Study
EGAS00001007288
-
Investigation of different library preparation and tissue of origin deconvolution methods for urine and plasma cfDNA methylome analysis
Study
EGAS00001007314
-
H3K27ac ChIP-seq in primary inflammatory (TPP) macrophages
Study
EGAS00001007562
-
Idiosyncratic and generic single nuclei and spatial transcriptional patterns in papillary and anaplastic thyroid cancers
Study
EGAS00001007574
-
Transcriptomic predictors of survival for palbociclib + endocrine therapy vs. capecitabine in aromatase inhibitor-resistant breast cancer from GEICAM/2013-02 PEARL
Study
EGAS00001008177
-
Lung_Cell_Atlas__Paediatric_RNA
Study
EGAS00001008299
-
Lung_Cell_Atlas__Paediatric_Spatial
Study
EGAS00001008300
-
single cell RNA-seq of peripheral blood from analysis in infants with MLL-rearranged Acute Lymphoblastic Leukemia
Dataset
EGAD00001007752
-
Annotated VCF Files for WGS of ASD Cohort with 68 Individuals from 22 families, enriched for recent shared ancestry
Dataset
EGAD00001008634
-
Bulk-tissue paired-end RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Dataset
EGAD00001007698
-
PELICAN33 Phenomic Dataset
Dataset
EGAD00001007800
-
Single-cell RNA sequencing data of human lymph node samples generated with BD Rhapsody
Dataset
EGAD00001010044
-
IMCISION RNAseq
Dataset
EGAD00001008127
-
DNA whole-exome sequencing data from patients with metastatic basal cell carcinoma
Dataset
EGAD00001008675
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow
Dataset
EGAD00001008788
-
Single nuclei RNA-Seq from 5 regions of the human fetal brain
Dataset
EGAD00001009303
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow sc Rhapsody
Dataset
EGAD00001009704
-
Targeted DNA panel sequencing analysis of PanNEN tumors of varying grades using custom and commercial panels
Dataset
EGAD00001008432
-
Single-cell RNA sequencing of SarBC-01 treated with Dexamethasone vs DMSO, with or without Matrigel.
Dataset
EGAD00001011155
-
Prediction of HLA genotypes using NGS data
Dataset
EGAD00001007733
-
Single-cell analysis reveals transcriptomic and epigenomic impacts on the maternal-fetal interface upon SARS-CoV-2 infection
Dataset
EGAD00001008770
-
COVID-19 Severity First Wave of Infection for Severe Patients in Madrid
Dataset
EGAD00001008464
-
Spatial multi-omic map of human myocardial infarction
Dataset
EGAD00001008952
-
cfMethyl-Seq
Dataset
EGAD00001009003
-
Roche Alzheimer's dataset
Dataset
EGAD00001009166
-
Blood neutrophils in COPD derive from activated progenitors in the bone marrow sc Seqwell
Dataset
EGAD00001008908
-
WGS of tumor and blood control samples of neuroblastoma
Dataset
EGAD00001009624
-
WES data for Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Dataset
EGAD00001015413
-
Roche multiple sclerosis dataset
Dataset
EGAD00001009169
-
Targetable NOTCH1 rearrangements in reninoma - WGS
Dataset
EGAD00001010888
-
RNA-seq of high-grade serous ovarian cancer in long-term survivors (MOCOG study)
Dataset
EGAD00001008537
-
Postmortem Single Nuclei and Bulk RNA-seq data of the Motor Cortex and Spinal Cord for Healthy, C9ALS and sALS Patients
Dataset
EGAD00001009686
-
CcRCC_metabolic_heterogeneity
Dataset
EGAD00001015780
-
Nasal epithelial cells of PCD and non-PCD patients grown at air-liquid interface for RNAseq analysis
Dataset
EGAD00001009498
-
Spatial transcriptome sequence data from cross section of cancer containing prostates
Dataset
EGAD00001008644
-
Total XVI RNAseq
Dataset
EGAD00001007530
-
RNA-seq dataset: Single-cell spatial analysis of pediatric high-grade glioma reveals a novel population of immunosuppressive and tumor-promoting SPP1+/GPNMB+ myeloid cells
Dataset
EGAD00001015450
-
RNA sequencing of 499 Greenlanders
Dataset
EGAD00001007717
-
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Dataset
EGAD00001007793
-
Enrichment of homologous recombination repair alteration in prostate cancer brain metastases
Dataset
EGAD00001008033
-
Platelets contain a repertoire of DNA fragments that map over the human nuclear genome, including tumour-derived DNA in patients with active malignancy.
Dataset
EGAD00001009856
-
Garvan/St Vincent’s Prostate Cancer Tissue and Data
Dataset
EGAD00001009066
-
RNA sequencing of end-stage kidney disease patients with COVID-19
Dataset
EGAD00001009752
-
scEC&T-seq manuscript data
Dataset
EGAD00001010071
-
Single-cell RNA-sequencing of rhabdomyosarcoma tumour tissue (2025-09-30)
Dataset
EGAD00001015713
-
DNA methylation sequencing profiles of 1538 breast tumors and 244 normal breast tissues
Dataset
EGAD00001007976
-
Somatic L1 retrotransposition in normal colorectal epthelium
Dataset
EGAD00001010183
-
Leiomyosarcoma Whole Genome Sequencing
Dataset
EGAD00001007722
-
Ither2 WXS dataset - Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Dataset
EGAD00001010178
-
Ither2 RNA-Seq dataset - Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Dataset
EGAD00001010179
-
Rare Disease Synthetic Dataset
Dataset
EGAD00001008392
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 6)
Dataset
EGAD00001010202
-
Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G4C2)n expression in C9orf72 ALS/FTD
Dataset
EGAD00001008674
-
INSPIRE multi-timepoint cfMeDIP dataset
Dataset
EGAD00001011312
-
Cancer-independent, second somatic NF1 mutation of normal tissues in neurofibromatosis type 1
Dataset
EGAD00001015398
-
scDNA-seq for 'Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma'
Dataset
EGAD00001015414
-
RNA-seq dataset
Dataset
EGAD00001007575
-
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Dataset
EGAD00001015357
-
Conserved interferon-gamma signaling and decreased immune exclusion programs in responses to immune checkpoint blockade therapy_CM38-RNA
Dataset
EGAD00001006282
-
Targeted sequencing of Human esophageal epithelium microbiopsies
Dataset
EGAD00001006969
-
Single-cell RNA sequencing data of peripheral blood mononuclear cells obtained from 30 ATL patients, 11 HTLV-1-infected asymptomatic carriers, and 4 healthy donors.
Dataset
EGAD00001007015
-
RNA-sequencing of meningiomas for integrative molecular classification.
Dataset
EGAD00001007494
-
Personalized analysis of ctDNA for detection of molecular residual disease and recurrence in a cohort of surgically treated patients with head and neck squamous cell carcinoma
Study
EGAS50000001018
-
VariantMedium: Sensitive and generalizable somatic point mutation calling with 3D DenseNets trained and evaluated on experimental confirmation data
Study
EGAS00001007633
-
Metabolomic and microbiome profiling reveals personalized risk factors for coronary artery disease
Study
EGAS00001005342
-
H3Africa - Consortium WGS
Study
EGAS00001005972
-
Chromosomal instability shapes the tumor microenvironment of oesophageal adenocarcinoma via a cGAS–chemokine–myeloid axis
Study
EGAS50000001561
-
Privacy Notice for the Account User
Documentation
data-protection/privacy-notice/ega-user-account
-
Privacy Notice for Helpdesk service
Documentation
data-protection/privacy-notice/ega-helpdesk
-
Profiling RNA Translation in Pediatric Medulloblastoma
Study
phs003446
-
Shedding light over COVID-19 susceptibility and severity
Blog
covid-19-susceptibility-and-severity
-
Discover Cancer Image Europe, the first release of the EUCAIM platform to fuel cancer research and data sharing
Blog
discover-cancer-image-europe
-
The Dutch Microbiome Project Batch 2
Dataset
EGAD00001007501
-
ARID1A Mutations in Endometriosis-Associated Ovarian Carcinomas
Study
EGAS00000000075
-
DO NOT USE - Whole genome sequencing of SI-NETs from six patients
Study
EGAS00001005009
-
St. Jude Children’s Research Hospital – Washington University Pediatric Cancer Genome Project Steering Committee
Dac
EGAC00001000044
-
Genetic mechanisms of resistance to chemotherapy in breast cancer
Dataset
EGAD00001000264
-
Somatic mutations, clonal architecture and genomic evolution in multiple myeloma
Dataset
EGAD00001000339
-
ICGC Prostate Cancer Whole Genome Sequencing
Dataset
EGAD00001000891
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Dataset
EGAD50000000277
-
SNP Genotype Data: Subpopulations of Filipino, Malaysian, and Papua New Guinea
Study
EGAS50000000044
-
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Study
EGAS50000000021
-
Nurminen et al ("GP2Men") Study Primary and Metastatic Prostate Cancer Whole Genome Sequence Data
Study
EGAS50000000005
-
Whole exome sequencing of pediatric soft tissue sarcoma PDX models
Study
EGAS50000000048
-
Processed Chromium Single Cell GEX, CSP and VDJ data from intestinal plasma cells of untreated celiac disease patients
Dataset
EGAD50000000339
-
Targeted re-sequencing of multi-region sampled tumors in PDAC
Study
EGAS50000000239
-
Alterations in the gut microbiome in inflammatory arthritis implicate key taxa and metabolic pathways across arthritis phenotypes
Study
EGAS00001005525
-
PARK7/DJ-1 deficiency modulates microglial activation in response to LPS-induced inflammation
Study
EGAS50000000202
-
ATAC sequencing of Treg cell subsets
Study
EGAS50000000457
-
Long read mRNA sequencing of human neural retinal samples - Usher syndrome transcript landscape
Dataset
EGAD50000000720