-
Dynamic N6-methyladenosine Epitranscriptomic Landscape in Lung Adenocarcinoma
Study
EGAS00001005524
-
Whole genome sequence and RNA-seq data from paired tumour and germline samples from mesothelioma patients.
Study
EGAS00001005196
-
Dissecting the Spatial Heterogeneity of Single Circulating Tumor Cells in Hepatocellular Carcinoma
Study
EGAS00001005204
-
Multimodal single-cell and bulk glioma analyses
Study
EGAS00001005300
-
Orphan_Tumour_Study___familial_neuroblastoma
Study
EGAS00001002171
-
Whole genome analysis of pediatric patients with medulloblastoma
Study
EGAS00001006653
-
How to use the EGA search box
Documentation
discovery/metadata/search-box
-
Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas
Study
EGAS00001002533
-
Whole exome sequencing for primary lung adenocarcinoma samples
Study
EGAS00001003680
-
Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552
-
Germline MBD4 Mutations and Predisposition to Uveal Melanoma
Study
EGAS00001003941
-
Comprehensive genomic and transcriptomic analysis of three synchronous primary tumours and a recurrence from a head and neck cancer patient
Study
EGAS00001004857
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
ICGC Oesophageal adenocarcinoma - normal samples
Study
EGAS00001000723
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Study
EGAS00001002761
-
National Human Genome Research Institute Tumor Sequencing Project (TSP) - Lung Adenocarcinoma
Study
phs000144
-
Neuroblastoma Genome-Wide Association Study (NBL-GWAS)
Study
phs000124
-
A Whole Genome Association Scan for Myopia and Glaucoma Endophenotypes using Twin Studies
Study
phs000142
-
CIDR: Discovery, Biology, and Risk of Inherited Variants in Glioma
Study
phs002250
-
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
-
OMRF SLEGEN GWAS Data from European-American Women with Lupus
Study
phs000202
-
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Study
phs000206
-
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
-
National Cancer Institute Cancer Genome Characterization Initiative (CGCI)
Study
phs000235
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Study
phs000238
-
National Eye Institute (NEI) Ocular Hypertension Treatment Study (OHTS)
Study
phs000240
-
Foregut Microbiome in Development of Esophageal Adenocarcinoma
Study
phs000260
-
Genome-Wide Association Study of Celiac Disease
Study
phs000274
-
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
-
The Primary Open-Angle Glaucoma Genes and Environment (GLAUGEN) Study
Study
phs000308
-
Towards a Genomic Understanding of Myeloma
Study
phs000348
-
Genome-Wide Analysis of Diffuse Large B-Cell Lymphoma (De Novo and Derived from the High Grade Transformation of Follicular Lymphoma)
Study
phs000328
-
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
-
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
-
High density copy number analysis and whole exome sequencing of unselected chronic lymphocytic leukemia cases and of paired chronic lymphocytic leukemia and Richter Syndrome cases
Study
phs000364
-
The Mutational Landscape of Head and Neck Squamous Cell Carcinoma
Study
phs000370
-
Genentech whole genome and transcriptome sequencing of four hepatocellular carcinoma patients
Study
phs000384
-
Whole Genomic Sequencing of Nine Primary Colorectal Adenocarcinoma Tumor/Germline Pairs
Study
phs000374
-
The Genomic Analysis of Medulloblastoma
Study
phs000409
-
Whole Exome Sequencing for Colorectal Cancer
Study
phs000410
-
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Study
phs000419
-
Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C)
Study
phs000430
-
The mutational characterization of adenoid cystic carcinoma
Study
phs000612
-
Whole Exome Sequencing of Primary Mediastinal B-cell Lymphoma
Study
phs000450
-
Melanoma Genome Sequencing Project
Study
phs000452
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in NEIGHBOR Samples
Study
phs000458
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in GLAUGEN Samples
Study
phs000461
-
Genome-Wide Analysis of Splenic Marginal Zone Lymphoma
Study
phs000502
-
Genomic Sequencing of Lung Adenocarcinoma
Study
phs000488
-
Whole-Genome and Exome Sequencing in clear-cell Renal Cell Carcinoma (ccRCC)
Study
phs000491
-
Medulloblastoma exome sequence analysis
Study
phs000504
-
Gene Fusion Discovery through RNA Sequencing of Human Glioblastoma Stem Cell Lines
Study
phs000505
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Genome Sequencing of Pancreatic Ductal Adenocarcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000516
-
Study of Melanoma Risk in Australia and the United Kingdom
Study
phs000519
-
Exome Sequencing of Pleuropulmonary Blastoma
Study
phs000543
-
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Study
phs000545
-
A Genome-Wide Association Study in Breast Cancer Patients from the Prospectively Randomized SUCCESS Trial
Study
phs000547
-
Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing
Study
phs000550
-
Genomic Characterization of Meningiomas
Study
phs000552
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Study
phs000558
-
Population Architecture Using Genomics and Epidemiology (PAGE): Epidemiologic Architecture for Genes Linked to Environment (EAGLE) - BioVU Cancer Project
Study
phs000559
-
The Genetic Landscape of Mutations in Burkitt Lymphoma
Study
phs000562
-
The Genomics of Pilocytic Astrocytoma Formation in Neurofibromatosis Type 1
Study
phs000563
-
Genetic Heterogeneity of Diffuse Large B Cell Lymphoma
Study
phs000573
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Strong Heart Study (SHS) and Strong Heart Family Study (SHFS)
Study
phs000580
-
Exome Sequencing of Esophageal Adenocarcinoma
Study
phs000598
-
Genomic Sequencing of Cervical Cancers
Study
phs000600
-
Identification of Targetable FGFR Gene Fusions in Diverse Cancers
Study
phs000602
-
Genomic Analysis of Pediatric Low Grade Gliomas
Study
phs000614
-
University of North Carolina at Chapel Hill (UNC) Hepatocellular Carcinoma Study by Exome Sequencing (HCCSES)
Study
phs000627
-
Characterization of a Metastatic Cervical Cancer Patient and HPV18 Integration Using Next Generation Sequencing
Study
phs000628
-
Genetic Epidemiology of Chronic Lymphocytic Leukemia
Study
phs001568
-
Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)
Study
phs000652
-
Germline Sequencing for Aggressive Prostate Carcinoma
Study
phs000661
-
University of Michigan Clinical Sequencing Exploratory Research (CSER)
Study
phs000673
-
Osteosarcoma Genomics
Study
phs000699
-
Genome Sequencing Reveals That RAD50 Hypomorphism Results in Enhanced Sensitivity to Checkpoint Kinase Inhibition Combined with Chemotherapy
Study
phs000706
-
Genomic and Transcriptomic Landscape of Fibrolamellar Hepatocellular Carcinoma
Study
phs000709
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
Pathogenesis and Immunity in Endemic Burkitt Lymphoma
Study
phs001282
-
Sequencing of Cervical Cancer
Study
phs000723
-
Rare Cancer Tumors Project
Study
phs000725
-
Solution-based exome capture and HiSeq2000-based massively parallel sequencing of Follicular Lymphoma
Study
phs000729
-
A Genome-wide Association Study (GWAS) of Risk for Osteosarcoma
Study
phs000734
-
Identification of Recurrent SMO and BRAF Mutations in Ameloblastomas
Study
phs000739
-
Whole Genome Sequencing of Waldenstrom's Macroglobulinemia
Study
phs000740
-
Relating Clinical Outcomes in Multiple Myeloma to Personal Assessment of Genetic Profile
Study
phs000748
-
Genomic sequencing of Ewing's Sarcoma
Study
phs000768
-
Bladder Chemotherapy Responders
Study
phs000771
-
Post-liver transplant recurrent human hepatocellular carcinoma study (RHCCS)
Study
phs000782
-
Exome Sequencing Analysis of Cutaneous Squamous Cell Carcinoma
Study
phs000785
-
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Study
phs000801
-
Genomic Sequencing of Ewing Sarcoma
Study
phs000804
-
Discovery of Novel Melanoma Predisposing Mutations by Exome Sequencing
Study
phs000823