-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
Chromothripsis in human breast cancer (HIPO K26K/H017/A017)
Study
EGAS00001004662
-
Prognostic and therapeutic significance of leukemia subtypes and minimal residual disease measurements in pediatric acute lymphoblastic leukemia treated with contemporary risk-directed trial: a cohort study
Study
EGAS00001004739
-
Tumor from individual with germline POLD1 L474P
Dataset
EGAD00001009281
-
One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids
Study
EGAS00001006886
-
RNA-sequencing from duodenal bipsies of Celiac disease patients
Dataset
EGAD50000000491
-
Clonal Evolution in Patients with Chronic Lymphocytic Leukemia
Study
phs001091
-
Identification and phenotypic characterization of neoantigen-specific cytotoxic CD4+ T cells in endometrial cancer
Study
JGAS000766
-
Identification of Recurrent SMO and BRAF Mutations in Ameloblastomas
Study
phs000739
-
Large Scale Meta-analysis Characterizes Genetic Architecture for Common Psoriasis-associated Variants
Study
phs001306
-
Splenic_Marginal_Zone_Lymphoma_with_villous_lymphocytes_exome_sequencing
Study
EGAS00001000139
-
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Study
EGAS00001006916
-
Spatial whole exome sequencing of metastatic melanoma
Dataset
EGAD00001005819
-
The transcriptomic response of skeletal muscle in life-long high-level trained and untrained men and women after acute exercise
Dataset
EGAD00001008663
-
Genomic characterisation of SDH deficient renal cell carcinoma - RNA
Dataset
EGAD00001008470
-
WGS sequencing of an ES tumor sample
Dataset
EGAD00001015607
-
Dataset for liposarcoma-RNA
Dataset
EGAD00001008854
-
Cell-free DNA Methylome Analysis Enables Early Preeclampsia Prediction
Dataset
EGAD00001010159
-
A Prospective Natural History Study of Diagnosis, Treatment and Outcomes of Children with SCID Disorders
Study
phs001392
-
NIDA Genetic Epidemiology of Opioid Dependence in Bulgaria (GEODB)
Study
phs001804
-
PBMCs of HCC Patients treated with anti-PD1 ICB
Dataset
EGAD00001006645
-
Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Dataset
EGAD00001001691
-
A Genome-Wide Association Study of Lung Cancer Risk
Study
phs000336
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs000379
-
Structure and Diversity of Urinary Cell-Free DNA Informative of Host-Pathogen Interactions in Human Urinary Tract Infection
Study
phs001564
-
Gene expression signatures associated with chronic endometritis revealed by RNA sequencing
Study
JGAS000621
-
A Genomic Atlas of Systemic Interindividual Epigenetic Variation in Humans (GTEx)
Study
phs001746
-
The Heterogeneity Study of HeLa S3 Cells Based on Full-Length Single-Cell RNA-Seq
Study
phs001029
-
Spatial profiling of hepatocellular carcinoma identifies distinct tumor and immune micro-ecosystems related to patient outcomes
Study
EGAS50000001474
-
Whole genome sequencing of PDAC tissues an PDOs
Study
EGAS50000000193
-
4 - transcriptome (.bam) files, 2 -called somatic mutations (.vcf) files and 2 coverage (.csv) files
Dataset
EGAD50000002055
-
Longitudinal multi-omics support immunotrhrombosis as the molecular force behind increased post-acute complication risk
Study
EGAS50000001430
-
Exome_sequencing_in_patients_with_cardiac_arrhythmias
Study
EGAS00001000063
-
Complex structural variation patterns in pediatric solid tumors
Study
EGAS00001007565
-
Genomic characterisation of SDH deficient renal cell carcinoma - WGS
Dataset
EGAD00001008469
-
Whole genome sequencing data of relapsed paediatric KMT2A-rearranged acute lymphoblastic leukemia
Dataset
EGAD50000001593
-
Long-read mRNA sequencing of retinal organoids
Dataset
EGAD50000000100
-
Exome reads
Dataset
EGAD00001003841
-
Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants
Dataset
EGAD00001004838
-
Amplicon sequencing of adenoma to carcinoma paired samples from colon
Dataset
EGAD00001004848
-
Exome and RNA seq data for female patient
Dataset
EGAD00001005249
-
A Personalized Neoantigen Vaccine Generates Anti-Tumor Immunity in High-Risk Renal Cell Carcinoma
Study
phs003710
-
Implementation of the GDPR
Documentation
about/privacy-notice
-
Gut microbiome dynamics unravelled with metagenomics sequencing
Blog
gut-microbiome-dynamics-unravelled
-
Thymic epithelial transplantation for complete DiGeorge syndrome: RNA (2025-07-22)
Dataset
EGAD00001015648
-
Gastric cancer RNA-seq data
Dataset
EGAD00001003448
-
Giant congenital nevi exome sequencing
Dataset
EGAD00001006283
-
Tremelimumab +/- durvalumab in combination with paclitaxel as immune induction in metastatic urothelial cancer: clinical and translational results of the ICRA trial
Study
EGAS50000001574
-
Exome-wide mutation analysis of cell-free DNA to simultaneously monitor the full spectrum of cancer treatment outcomes
Study
EGAS00001005906
-
Somatic mutations, clonal architecture and genomic evolution in multiple myeloma
Dataset
EGAD00001000339
-
Atezolizumab Plus Personalized Neoantigen Vaccination in Patients with Urothelial Cancer: a Phase 1 Trial
Study
phs003922
-
Foregut Microbiome in Development of Esophageal Adenocarcinoma
Study
phs000260
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
Type 1 Diabetes Genetics Consortium (T1DGC): Multi-Ethnic ImmunoChip Study
Study
phs002468
-
Cell-Free, Methylated DNA in Blood Samples Reveals Tissue-Specific, Cellular Damage from Radiation Treatment
Study
phs003290
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Multimodal Developmental Neurogenetics of Females
Study
phs002043
-
International Consortium on the Genetics of Systemic Lupus Erythematosus (SLEGEN)
Study
phs000216
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Genomics of Autism Spectrum Disorder (GASD)
Study
phs002509
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA)
Study
phs001894
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Simons Searchlight
Study
phs002512
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II)
Study
phs002042
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Study of Autism Genetics Exploration (SAGE)
Study
phs001740
-
Genomic Architecture of Progression and Treatment Response in AMD
Study
phs001046
-
Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG)
Study
phs002004
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Genetic Resource Exchange
Study
phs001766
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: The Autism Simplex Collection (TASC)
Study
phs001741
-
Utility of Capillary Blood in Gene Expression Studies
Study
phs003496
-
The Chromatin Landscape of Pathogenic Transcriptional Cell States in Rheumatoid Arthritis
Study
phs003417
-
Plasma-Seq of patients with metastatic prostate cancer
Study
EGAS00001000451
-
deep-learning-powered tissue deconvolution for cfDNA
Study
EGAS00001007213
-
Mechanisms of Restoring T Cell Immunity after Cure of Chronic Viral Infection
Study
phs002510
-
Genomic Analysis of Prostate Tumor Heterogeneity in Metastasis
Study
phs003404
-
Single-Cell Transcriptomic Analysis of Kaposi Sarcoma
Study
phs003800
-
Rapid brain tumor classification from sparse epigenomic data
Study
EGAS50000000559
-
Whole-genome array data for 42 Roma and 52 non-Roma from Czech Republic
Dataset
EGAD50000001103
-
JIA family
Dataset
EGAD00001004806
-
RNA Sequencing of mCRC xenografts under cetuximab treatment.
Dataset
EGAD00001005185
-
Cross-site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms of CIMAC-CIDC Network
Study
phs002295
-
Genome-Wide Association Study of Hypertriglyceridemia in Mexicans
Study
phs000618
-
CRU-Ukrainian National Research Center for Radiation Medicine Trio Study
Study
phs001163
-
Whole genome sequencing generated from metastatic gliosarcoma patient samples
Dataset
EGAD00001005745
-
Single cell sequencing data from Shwachman-Diamond syndrome bone marrow samples
Dataset
EGAD00001006799
-
Reliable detection of somatic mutations in single DNA molecules from sperm
Dataset
EGAD00001007028
-
Lowpass whole genome sequencing of single circulating tumor cells (CTCs) in ALK-rearranged non-small-cell lung cancer resistant to ALK inhibitors
Dataset
EGAD00001007700
-
Embryonal Rhabdomyosarcoma sequencing data
Dataset
EGAD00001007939
-
Characterization of mutational signatures in human cancer cell lines reveals episodic APOBEC mutagenesis
Dataset
EGAD00001004202
-
Long-Term Outcome in Offspring and Mothers of Dexamethasone-Treated Pregnancies at Risk for Classical Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Study
phs001317
-
NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Study
phs001515
-
FLG LoF Variants are Associated with Atopic Dermatitis in an Early-Life Prospective Cohort
Study
phs003489
-
Transcriptome sequencing of fibroblast-dependent alveolar organoids derived from patient-specific iPS cells with SFTPC^Y104H variant and their gene-corrected (monoallelic wild type SFTPC) ones.
Study
JGAS000617
-
Access to "A Spatially Resolved Single-Cell Atlas of the Human Fetal Olfactory System"
Dac
EGAC50000000688
-
Efficacy of asciminib in acute lymphoblastic leukaemia (ALL) patient derived NUP214::ABL1 xenografts.
Study
EGAS50000000957
-
Eribulin efficacy in platinum-resistant and refractory high-grade serous ovarian cancer patient-derived xenograft models
Study
EGAS50000000152
-
RNA sequencing from patient-derived intestinal organoids
Study
EGAS50000000338
-
NGS sequencing data of archival FFPE tumor tissue
Dataset
EGAD50000001371
-
Targeted_sequencing_of_genes_recurrently_mutated_in_AML___part2
Study
EGAS00001000570
-
Whole genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes
Study
EGAS00001004379
-
Gut microbiota analysis after 3months probiotic-like bacteria or placebo treatment in subjects with metabolic syndrome
Study
EGAS00001003585
-
The distinct DNA methylome of acute lymphoblastic leukemia
Study
EGAS00001005203
-
Whole genome sequencing in prime-edited human organoids
Dataset
EGAD00001006352