-
Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer
Study
EGAS00001005108
-
Single cell RNA sequencing of 33 primary colorectal cancer
Study
EGAS00001003779
-
Germline elongator mutations in sonic hedgehog medulloblastoma
Study
EGAS00001004126
-
Single cell multi-omics analysis of chromothriptic medulloblastoma highlights genomic and transcriptomic consequences of genome instability
Study
EGAS00001005410
-
EGA synthetic data
Documentation
synthetic-data
-
How to use the EGA search box
Documentation
discovery/metadata/search-box
-
Submission FAQ
Documentation
submission/metadata/submission/FAQ
-
Projects
Documentation
about/projects-and-funders/projects
-
GA4GH
Documentation
about/projects-and-funders/ga4gh
-
Federated EGA
Documentation
about/projects-and-funders/federated-ega
-
Catalog Statistics
Documentation
about/statistics/catalog
-
Immune induction strategies to enhance the sensitivity to PD-1 blockade in metastatic triple negative breast cancer: the TONIC-trial
Study
EGAS00001003535
-
Complex structural variation patterns in pediatric solid tumors
Study
EGAS00001007565
-
Immune and clinicopathological features predict HER2-positive breast cancer prognosis in the neoadjuvant NeoALTTO and CALGB 40601 trials
Study
EGAS00001007563
-
560 whole-genome sequenced breast cancers
Study
EGAS00001001178
-
The BC Cancer Agency's Personalized Onco-Genomics Project
Study
EGAS00001001159
-
Loss of SDHB promotes dysregulated iron homeostasis, oxidative stress and sensitivity to ascorbate
Study
EGAS00001005279
-
BRCA-deficiency/HRD in individuals with HBOC
Study
EGAS00001007258
-
PanCuRx Translational Research Initiative
Study
EGAS00001002543
-
Spatial atlas of clonal copy number alterations in co-existing benign and malignant tissue
Study
EGAS00001006124
-
Dissecting intratumor heterogeneity of nodal B cell lymphoma on the transcriptional, genetic, and drug response level
Study
EGAS00001004335
-
Genomic Rearrangements in Pediatric Cancer
Study
EGAS00001005312
-
Proteomic Analysis of Non-Muscle Invasive and Muscle Invasive Bladder Cancer Highlights Distinct Subgroups With Metabolic, Matrisomal, and Immune Hallmarks
Study
EGAS00001007290
-
Finding structural variation and functional consequences from primary acute myeloid leukemia cells with complex karyotype (CK-AML) at the single-cell level
Study
EGAS00001007436
-
METABRIC
Study
EGAS00000000083
-
Breast Cancer PDTX Encyclopaedia
Study
EGAS00001001913
-
Single cell genomic variation induced by mutational processes in cancer
Study
EGAS00001006343
-
CNV detection in targeted NGS panel data
Study
EGAS00001002481
-
Combined gene expression and digital pathology identifies molecular mediators of T cell exclusion and immune suppression in ovarian cancer
Study
EGAS00001003487
-
Hereditary Cancer Diagnostics with I2HCP gene panel
Study
EGAS00001004316
-
Intratumoral plasma cells predict outcomes to PD-L1 blockade in non-small cell lung cancer
Study
EGAS00001005013
-
Berlin Neuroblastoma Dataset Update 2021
Study
EGAS00001005604
-
A dataset compiled as a resource a for orthogonal assessment of exon CNV calling in NGS data
Study
EGAS00001002428
-
Comprehensive genomic profiles of small cell lung cancer
Study
EGAS00001000925
-
Berlin Neuroblastoma Dataset
Study
EGAS00001004022
-
National Human Genome Research Institute Tumor Sequencing Project (TSP) - Lung Adenocarcinoma
Study
phs000144
-
Study of Addiction: Genetics and Environment (SAGE)
Study
phs000092
-
A Genome Wide Scan of Lung Cancer and Smoking
Study
phs000093
-
Whole Genome Association Study of Systemic Lupus Erythematosus
Study
phs000122
-
Neuroblastoma Genome-Wide Association Study (NBL-GWAS)
Study
phs000124
-
Cancer Genetic Markers of Susceptibility (CGEMS) Breast Cancer Genome-wide Association Study (GWAS) - Primary Scan: Nurses' Health Study - Additional Cases: Nurses' Health Study 2
Study
phs000147
-
National Institutes of Health The Cancer Genome Atlas (TCGA)
Study
phs000178
-
High Density SNP Association Analysis of Melanoma: Case-Control and Outcomes Investigation
Study
phs000187
-
Women's Health Initiative Clinical Trial and Observational Study
Study
phs000200
-
International Standards for Cytogenomic Arrays
Study
phs000205
-
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Study
phs000206
-
Cancer Genetic Markers of Susceptibility (CGEMS) Prostate Cancer Genome-Wide Association Study (GWAS) - Primary Scan (Stage 1) - PLCO Screening Trial
Study
phs000207
-
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
National Cancer Institute (NCI) TARGET: Therapeutically Applicable Research to Generate Effective Treatments
Study
phs000218
-
Population Architecture using Genomics and Epidemiology (PAGE): Multiethnic Cohort (MEC)
Study
phs000220
-
Development and Use of Network Infrastructure for High-Throughput GWA Studies
Study
phs000234
-
National Cancer Institute Cancer Genome Characterization Initiative (CGCI)
Study
phs000235
-
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
Study
phs000239
-
Whole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples
Study
phs000245
-
Genetic Determinants of Viral Clearance in HCV-Infected Populations
Study
phs000248
-
CALGB 80303:Genome-Wide Association Study of Advanced Pancreatic Cancer Patients - A Randomized Phase III trial of Gemcitabine Plus Bevacizumab versus Gemcitabine Plus Placebo in Patients with Advanced Pancreatic Cancer
Study
phs000250
-
National Human Genome Research Institute (NHGRI) GENEVA Genome-Wide Association Study of Venous Thrombosis (GWAS of VTE)
Study
phs000289
-
Whole genome and transcriptome sequencing of lung cancer patients and cell lines at Genentech
Study
phs000299
-
A Genome-Wide Association Study in Participants Experiencing Breast Cancer Events in High-Risk Postmenopausal Women Receiving Selective Estrogen Receptor Modulators on NSABP Trials P-1 and P-2. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000305
-
A Multiethnic Genome-wide Scan of Prostate Cancer
Study
phs000306
-
Discovery of Non-ETS Gene Fusions in Human Prostate Cancer using Next Generation RNA Sequencing
Study
phs000310
-
FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data
Study
phs000311
-
The Genomic Complexity of Primary Human Prostate Cancer
Study
phs000330
-
A Genome-Wide Association Study of Lung Cancer Risk
Study
phs000336
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
Genome-wide association study for Bladder Cancer Risk
Study
phs000346
-
Fred Hutchinson Cancer Research Center - Whole-Exome Sequencing of Hereditary Prostate Cancer Families
Study
phs000350
-
National Cancer Institute Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs000351
-
The genomic complexity of sporadic and inherited retinoblastoma with a matched orthotopic xenograft
Study
phs000352
-
Genome-Wide Association Studies in Upper Gastrointestinal Cancers (Asian)
Study
phs000361
-
California Pacific Medical Center Research Breast Health Cohort
Study
phs000395
-
Sequence Analysis of Mutations and Translocations Across Breast Cancer Subtypes
Study
phs000369
-
The Mutational Landscape of Head and Neck Squamous Cell Carcinoma
Study
phs000370
-
Whole Genomic Sequencing of Nine Primary Colorectal Adenocarcinoma Tumor/Germline Pairs
Study
phs000374
-
Genome-Wide Association Study of Breast Cancer in the African Diaspora - the ROOT study
Study
phs000383
-
Epigenetic Profiling of Human Colorectal Cancer
Study
phs000385
-
Division of Cancer Epidemiology and Genetics (DCEG) Imputation Reference Dataset
Study
phs000396
-
The Genetic Architecture of Smoking and Smoking Cessation
Study
phs000404
-
Whole Exome Sequencing for Colorectal Cancer
Study
phs000410
-
Temporal Dissection of Tumorigenesis in Primary Cancers
Study
phs000418
-
Whole Exome Sequencing of Chronic Lymphocytic Leukemia
Study
phs000435
-
Transcriptome sequencing across a prostate cancer cohort identifies PCAT-1, an unannotated lincRNA implicated in disease progression
Study
phs000443
-
Prostate Cancer Genome Sequencing Project
Study
phs000447
-
Melanoma Genome Sequencing Project
Study
phs000452
-
Exome Recapture and Sequencing of Prospectively Characterized Clinical Specimens From Cancer Patients
Study
phs001783
-
Estrogen Receptor Positive Breast Cancer: Aromatase Inhibitor Response Study
Study
phs000472
-
Identification of Cancer Predisposition Genes in Breast Cancer Families
Study
phs000480
-
Functionally Active Copy Number Variants Associated with Prostate Cancer Risk
Study
phs000487
-
Genomic Sequencing of Lung Adenocarcinoma
Study
phs000488
-
Medulloblastoma exome sequence analysis
Study
phs000504
-
Genomic Sequencing of Pediatric Rhaboid Cancers
Study
phs000508
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Rearrangements of the MAST Kinase and Notch Gene Families in Breast Cancer
Study
phs000513
-
Genome Sequencing of Pancreatic Ductal Adenocarcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000516
-
GWAS in African Americans, Latinos and Japanese
Study
phs000517
-
Study of Melanoma Risk in Australia and the United Kingdom
Study
phs000519
-
Expressed Pseudogenes in the Transcriptional Landscape of Human Cancers
Study
phs000525
-
Whole Genome and Exon Capture Sequencing of Bladder Cancers
Study
phs000535
-
Exome Sequencing of Pleuropulmonary Blastoma
Study
phs000543
-
A Genome-Wide Association Study in Breast Cancer Patients from the Prospectively Randomized SUCCESS Trial
Study
phs000547