-
Total RNA-seq of intestinal gluten tetramer+ and tetramer- CD4+ T-cells from celiac disease patients
Dataset
EGAD00001004146
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Dataset
EGAD00001004286
-
Whole-exome sequencing of additional thyroid disease cases (2018-08-13)
Dataset
EGAD00001004293
-
GIS-LUNGTCR1-2016_VAL-FASTQ
Dataset
EGAD00001001981
-
BLUEPRINT: RNA-seq for monocytes and neutrophils
Dataset
EGAD00001000675
-
RNA-seq, ChIP-seq, ATAC-seq files for PCGP SJERG
Dataset
EGAD00001002681
-
Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma.
Dataset
EGAD00001004795
-
Gene regulation of human CD4+ Treg ChM-seq
Dataset
EGAD00001004828
-
Clinical phenotypes/covariates
Dataset
EGAD00001005040
-
VCF files of Roma and non-Roma Romanians
Dataset
EGAD00001004982
-
Organoid Derivation Project TGS: Release 2
Dataset
EGAD00001004999
-
Organoid Derivation Project WGS: Release 1
Dataset
EGAD00001005000
-
Organoid Derivation Pilot: RNAseq
Dataset
EGAD00001005001
-
WES_localized non-small cell lung cancer (540 samples)_MDACC
Dataset
EGAD00001005956
-
WGBS for T-Cell and B-Cell, control and tumor
Dataset
EGAD00001005970
-
Total RNAseq in the sporadic ALS and healthy control motor cortex
Dataset
EGAD00001006022
-
PFA ependymoma study -WGS data
Dataset
EGAD00001006045
-
WGS paired B-Cell lymphoma cells sorted according to CD48
Dataset
EGAD00001006058
-
Whole exome sequencing analysis on patient-derived cervical cancer tissues and respective tumoroids
Dataset
EGAD00001006166
-
A Microwell Platform for High-Throughput Longitudinal Phenotyping and Selective Retrieval of Organoids
Study
phs003315
-
Error-corrected flow-based sequencing at whole genome scale and its application to circulating cell-free DNA profiling
Study
EGAS50000000844
-
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
-
Identification of Rare Germline Variants in Familial Patients with Non-medullary Thyroid Cancer
Study
phs001758
-
3/7 Psychiatric Genomics Consortium: Finding Actionable Variation
Study
phs003138
-
Identification of Cancer Predisposition Genes in Breast Cancer Families
Study
phs000480
-
Phase 2 Study of Nivolumab and Entinostat in Unresectable or Metastatic Cholangiocarcinoma and Pancreatic Adenocarcinoma
Study
phs003615
-
Single-Cell RNA-Seq Profiling of Peripheral Immune Responses to Severe Infection in Uganda
Study
phs004100
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Atherosclerosis Risk in Communities Study (ARIC)
Study
phs002988
-
A thymic ILC1-like progenitor with differentiation potential towards KIR+NKG2A- NK cells
Study
EGAS50000000760
-
Somatic rearrangements causing oncogenic ectodomain deletions of FGFR1 in squamous cell lung cancer
Study
EGAS50000001368
-
Personalized peptide vaccination among 173 patients with IDH wildtype glioblastoma: a retrospective analysis
Study
EGAS50000000449
-
Organoid BulkRNAseq
Study
EGAS50000000659
-
A thymic ILC1-like progenitor with differentiation potential towards KIR+NKG2A- NK cells - sc
Study
EGAS50000000790
-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
Inquiring the potential of donor derived CD19-CAR TSCM to treat B-cell malignancies.
Study
EGAS00001008119
-
Detection of mutational patterns in cell free DNA (cfDNA) of colorectal cancer by custom amplicon sequencing
Study
EGAS00001003382
-
mFAST-SeqS
Study
EGAS00001001133
-
Mutational signatures of aflatoxin
Study
EGAS00001002490
-
Targeted de-methylation of the FOXP3-TSDR
Study
EGAS00001004867
-
Tremelimumab +/- durvalumab in combination with paclitaxel as immune induction in metastatic urothelial cancer: clinical and translational results of the ICRA trial
Study
EGAS50000001574
-
IMvigor210 and IMmotion150 DAC
Dac
EGAC00001001493
-
IRSJD and Avgustinova Lab
Dac
EGAC00001003570
-
NHLBI TOPMed: Boston-Brazil Sickle Cell Disease (SCD) Cohort
Study
phs001599
-
Improving Transcriptome Fidelity Following Synovial Tissue Disaggregation
Study
phs002991
-
Human Tumor Atlas Network (HTAN)
Study
phs002371
-
Genomic Characterization of HPV+ Oropharyngeal Tumors
Study
phs003925
-
Amplicon sequencing of duodenal adenoma
Study
JGAS000352
-
Whole Genome Sequencing Analysis of Adult T-cell Leukemia/Lymphoma
Study
JGAS000320
-
WTCCC2 case-control study for Ulcerative Colitis
Study
EGAS00000000084
-
Whole genome sequencing of chondrosarcoma
Study
EGAS00001000505
-
Orthogonal proteogenomic analysis identifies the druggable PA2G4-MYC axis in 3q26 AML
Study
EGAS50000000347
-
Single nuclei RNAseq data from HGSOC primary tumour samples
Study
EGAS50000000249
-
A mathematical model of cell-free DNA fragment size reveals cancer-specific fragmentomic patterns
Study
EGAS50000001560
-
Multisite_Breast_Cancer_Whole_Genome
Study
EGAS00001000890
-
A comprehensive genetic map of cytokine responses in Lyme borreliosis
Study
EGAS50000000024
-
Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression
Study
EGAS00000000119
-
Breast cancer risk SNPs converge on estrogen receptor binding sites commonly shared between breast tumors to locally alter estrogen signalling output
Study
EGAS50000000008
-
Whole genome bisulfite sequencing of prostate cancer samples upon oral pimonidazole administration
Study
EGAS50000000069
-
Multiple myeloma treated with T-cell redirecting immunotherapies
Study
EGAS50000000546
-
SALTO: chromosomal copy number alterations to predict response to bevacizumab
Study
EGAS50000000711
-
Pediatric UBA1-mutated MDS Single-Cell Sequencing DAC
Dac
EGAC50000000947
-
Whole transcriptome sequencing of C1498 cells.
Dataset
EGAD50000002404
-
SCIMAP ACTUAL D0, D3, D6, D8, D14, D49
Dataset
EGAD50000002520
-
Integrated whole-genome and transcriptome sequencing reveals divergent evolutionary processes across biliary tract cancer subtypes (WGS data from biliary tract cancer molecular subtype study)
Dataset
EGAD50000002530
-
Whole-exome sequencing of intrahepatic cholangiocarcinoma tumors with matched normal tissue from the Medical Center – University of Freiburg
Dataset
EGAD50000001926
-
Variant calling dataset from the whole-exome study of sepsis and acute distress respiratory syndrome in Spain
Dataset
EGAD50000001613
-
Data from Shea et al Can Research 2025
Dataset
EGAD50000001334
-
CHIP panel sequencing of rheumatoid arthritis patients
Dataset
EGAD50000001300
-
WGS dataset of salivary gland tumor samples and control blood samples
Dataset
EGAD50000001192
-
mUM patient biopsies pre and post treatment with tebentafusp
Dataset
EGAD50000001258
-
Paired FastQ files from deep targeted DNA sequencing
Dataset
EGAD50000001267
-
CRITICS trial Whole Exome Sequencing (WES)
Dataset
EGAD50000001145
-
LRS - episignature samples
Dataset
EGAD50000001000
-
Expression quantitative trait loci influence DNA damage-induced apoptosis in cancer
Dataset
EGAD50000000941
-
GIST Comprehensive Cancer Panel
Dataset
EGAD50000000548
-
BipEx-Landen: Bipolar Exome Sequencing
Dataset
EGAD50000000307
-
Paired RNA sequencing of Thymic epithelial tumors - Additional Dataset
Dataset
EGAD50000000324
-
Korean WGS
Dataset
EGAD50000000346
-
BIOMIROX
Dataset
EGAD50000000443
-
IMpower133 (GO30081) clinical data and biomarker data
Dataset
EGAD50000000195
-
Spatial and temporal transcriptome analysis on human skeletal muscle regeneration
Dataset
EGAD50000000263
-
Whole exome sequencing of preneoplasia lung adenocarcinoma
Dataset
EGAD50000000397
-
singel cell RNAseq dataset for the study "Longitudinal Multi-Omics Study Reveals Molecular Drivers and Tumor Microenvironment in Extramedullary Multiple Myeloma"
Dataset
EGAD50000000053
-
Human Brain Small Extracellular Vesicles Contain Selectively-Packaged, Full-Length mRNA
Dataset
EGAD50000000042
-
Mutational consequences of precancerous liver disease
Dataset
EGAD00001004105
-
Multi-omics datasets (WES, RNA-seq) of mesothelioma MIST2 study, a phase II CDK4/6 (abemaciclib) clinical trial
Study
EGAS50000001823
-
DNA repair knockouts
Dataset
EGAD00001006777
-
GENOMIC INSTABILITY IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER
Study
EGAS00001002477
-
Whole_Genome_Sequencing_OMELib__Cord_blood_
Study
EGAS00001007453
-
Testing_the_feasibility_of_genome_scale_sequencing_in_routinely_collected_FFPE_cancer_specimens_versus_matched_fresh_frozen_samples
Study
EGAS00001000173
-
Chondromyxoid_fibroma
Study
EGAS00001000533
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001001293
-
Sequencing_melanoma_germlines
Study
EGAS00001002081
-
Failure of Differentiation of the Rhombic Lip Constitutes Medulloblastoma
Study
EGAS00001005826
-
A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome
Study
EGAS00001006203
-
GWAS genotype data of Japanese
Study
EGAS00001006423
-
Single cell study of infant leukemias
Dataset
EGAD00001007853
-
A life history of colorectal cancer metastases
Dataset
EGAD00001007503
-
RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics
Dataset
EGAD00001007754
-
Dataset-linking-WGS-via-README-for-EGAS00001004884
Dataset
EGAD00001007669