-
scRNA-seq of LN and lymphoma stroma
Study
EGAS00001005732
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study
Study
EGAS00001001709
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
Clinical outcomes in ctDNA-positive urothelial carcinoma patients treated with adjuvant immunotherapy
Study
EGAS00001004997
-
an integrated molecular study of clear cell renal cell carcinoma (ccRCC) including whole-genome/exome and RNA sequencing as well as array-based gene expression/copy-number/methylation analyses
Study
EGAS00001000509
-
Dynamics of genome architecture and chromatin function during human B cell differentiation and neoplastic transformation
Study
EGAS00001004763
-
Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Study
EGAS00001007053
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
Single-cell RNA sequencing on single CD45+ immune cells isolated from peripheral blood, lymphnode, ascites, tumour and adjacent normal tissues from six hepatocellular carcinoma patients.
Study
EGAS00001003449
-
Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy
Study
EGAS00001004422
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
Single-cell profiling maps the spectrum of crosstalk between glioma cells and tumor associated macrophages
Study
EGAS00001002185
-
Leeds Melanoma Cohort (LMC) gene expression study
Study
EGAS00001002922
-
A single-cell atlas of human glioma
Study
EGAS00001003845
-
Genome Landscape of Primary Pancreatic Ductal Adenocarcinoma
Study
EGAS00001000154
-
The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH
Study
EGAS00001004285
-
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Study
EGAS00001002936
-
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
-
Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Study
EGAS00001005395
-
SPECIAL: Dissecting the melanoma ecosystem one cell at the time during immunotherapy
Study
EGAS00001006488
-
Single cell RNA-sequencing of GSCs and GBM tumours
Study
EGAS00001004656
-
Molecular subsets in renal cancer determine outcome to checkpoint and angiogenesis blockade
Study
EGAS00001004353
-
Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients
Study
EGAS00001001024
-
Multimodal single-cell and bulk glioma analyses
Study
EGAS00001005300
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck
Study
EGAS00001005450
-
PanCuRx Translational Research Initiative
Study
EGAS00001002543
-
Initial whole genome sequencing of plasma cell neoplasms in First Responders exposed to the World Trade Center attack of September 11, 2001
Study
EGAS00001004467
-
Integrated genetic analysis of primary CNS lymphoma
Study
EGAS00001007222
-
Gene fusion and transcriptomic landscapes of sarcomas
Study
EGAS00001002189
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
Genomic_characterisation_of_MGUS__
Study
EGAS00001004124
-
Mongolia Western HCC
Study
EGAS00001005364
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Neuroblastoma and adrenal gland single-cell study
Study
EGAS00001004388
-
Berlin Neuroblastoma Dataset
Study
EGAS00001004022
-
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
-
Study of complex rearrangements and mutational signatures in neuroblastoma heterogeneous risk groups.
Study
EGAS00001006983
-
Molecular determinants of response to PD-L1 blockade across tumor types
Study
EGAS00001004343
-
VIKING Health Study - Shetland
Study
EGAS00001003872
-
How to use the EGA search box
Documentation
discovery/metadata/search-box
-
High-resolution lung adenocarcinoma expression subtypes identify tumors with dependencies on MET, CDK4, CDK6, and PD-L1
Study
EGAS00001006461
-
Clinical activity and molecular correlates of response to atezolizumab alone or in combination with bevacizumab versus sunitinib in renal cell carcinoma
Study
EGAS00001002928
-
Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552
-
ICGC Oesophageal adenocarcinoma - normal samples
Study
EGAS00001000723
-
Integrated genomic analyses reveal molecular correlates of clinical response and resistance to atezolizumab in combination with bevacizumab in advanced hepatocellular carcinoma
Study
EGAS00001005503
-
Clonal dominance defines metastatic dissemination in pancreatic cancer
Study
EGAS00001006358
-
T cell reactivity of MHC epitopes
Study
EGAS00001006445
-
Integrative analysis of exome-seq, RNA-seq, ATAC-seq (bulk and single-cell), and Hi-C data generated from 3-D spatially mapped samples acquired during surgical resection from 10 patients diagnosed with IDH-WT glioblastoma
Study
EGAS00001006785
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET)
Study
EGAS00001003813
-
Single-nuclei gene-expression analysis of pheochromocytoma and paraganglioma links tumor subtypes with tumor microenvironment
Study
EGAS00001005861
-
Deciphering the aggressive nature of morphoeic basal cell carcinoma
Study
EGAS00001001915
-
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