-
Cell Type-Specific and Disease-Associated eQTL in the Human Lung
Study
phs003521
-
Single Cell Genotypic and Phenotypic Analysis of Measurable Residual Disease in Acute Myeloid Leukemia
Study
phs003233
-
Trisomy 21 Dosage Compensation Map (T21DoCoMap)
Study
phs002397
-
Diagnostic Genomic Analysis is Prognostic in AYA ALL Patients Treated on a MRD-Stratified Paediatric Protocol
Study
EGAS50000000752
-
Ultra-sensitive tumor-informed ctDNA monitoring of treatment response in advanced esophagogastric cancer patients
Study
EGAS50000001224
-
Identification of RNA biomarkers in Parkinson's disease patients
Study
JGAS000119
-
Plasma-Seq of patients with metastatic prostate cancer
Study
EGAS00001000451
-
Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2
Study
EGAS00001003973
-
RNA sequencing data from glioblastoma primary cell lines treated with indisulam data access committee
Dac
EGAC50000000407
-
RNAseq of GEPARSIXTO
Dataset
EGAD00001010201
-
A spatial human thymus cell atlas mapped to a continuous tissue axis
Dataset
EGAD00001015384
-
Non-Coding Autoimmune Risk Variant Defines Role for ICOS in T Peripheral Helper Cell Development
Study
phs003448
-
Frequent post-treatment monitoring of colorectal cancer using individualized ctDNA validated by multi-regional molecular profiling
Study
JGAS000243
-
Capturing disease severity in LIS1-lissencephaly reveals proteostasis dysregulation in patient-derived forebrain organoids
Study
EGAS00001008227
-
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Study
EGAS00001004440
-
The University of Hong Kong Intestinal Metaplasia Organoids Study
Study
EGAS00001007899
-
Idiopathic Pulmonary Fibrosis Network (IPFNet) Sildenafil Trial of Exercise Performance in Idiopathic Pulmonary Fibrosis (IPFNet-STEP-IPF-BioLINCC)
Study
phs004085
-
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
-
Whole exome sequencing of a representative cohort of AML
Dataset
EGAD00001007580
-
Targeted de novo phasing and long-range assembly by template mutagenesis
Dataset
EGAD00001008444
-
59 CLPD-NK cases WGS & WTS data
Dataset
EGAD00001008558
-
TCR- and BCR-sequencing data for The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Dataset
EGAD00001003985
-
Deep amplicon sequencing to infer malignant clonal populations for The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Dataset
EGAD00001003986
-
Single-cell RNA-sequencing of CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) from a Phase I clinical study in paediatric ALL: CARPALL
Dataset
EGAD00001010018
-
Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas
Study
phs001403
-
The International Consortium for Prostate Cancer Genetics Genome Wide Association Study of Familial Prostate Cancer
Study
phs000733
-
Systems Analysis of the PfSPZ Vaccine in Kenyan Infants
Study
phs002196
-
Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Study
phs000413
-
Single-Cell Analysis of CD19-Specific CAR T Cell Treatment of Relapsed/Refractory CD19+ Acute Lymphoblastic Leukemia
Study
phs002966
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Study
phs000422
-
Genotyping NIGMS CEPH Samples from the United States, Venezuela, and France
Study
phs000268
-
Microvascular Permeability, Inflammation, and Lesion Physiology in Endometriosis: A Microphysiological Systems Approach
Study
phs003326
-
Stockholm-Tartu Atherosclerosis Reverse Network Engineering Task (STARNET)
Study
phs001203
-
Impact of Genetic Variation on Response to GO Therapy in COG-AML Trials AAML03P1 and AAML0531
Study
phs003490
-
EGA account management
Documentation
how-to-manage-your-account
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines
Study
EGAS00001002998
-
Matching of actionable mutations with therapies in cancer patients: comparison of three commercial decision support platforms
Study
EGAS00001004383
-
Exploration of coding and non-coding variants in cancer using GenomePaint.
Study
EGAS00001004669
-
Environmental Arsenic and Diabetes Mellitus (Chihuahua Cohort)
Study
phs002139
-
Treatment of Pulmonary Hypertension and Sickle Cell Disease with Sildenafil Therapy (Walk-PHaSST)
Study
phs002383
-
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics
Study
phs001496
-
Prediction of Resistance and Sensitivity to HER2 Targeted Therapy in the Neoadjuvant Setting
Study
phs003275
-
Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2
Dataset
EGAD00001005448
-
Whole Exome sequencing of colorectal cancer patients (SG-BULK)
Dataset
EGAD00001008543
-
Whole genome sequencing delineates regulatory and other genic variants in early onset cardiomyopathy
Dataset
EGAD00001008477
-
WXS and RNA-seq raw sequence data for TG project
Dataset
EGAD00001007989
-
scRNA-seq of total bone marrow and T cells from multiple myeloma long-term survivors
Dataset
EGAD00001010025
-
Influence of the Microbiome on Epigenetic Mechanisms in IBD
Dataset
EGAD00001011066
-
Genome-Wide Association Study of Leprosy and Dapsone Hypersensitivity Syndrome (DHS) in Chinese population
Study
phs000217
-
A Genome-Wide Association Comparative Analysis of Response of AF Patients to Rate Control Therapy; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000439
-
Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia Genomes
Study
phs000201
-
Polycystic Ovary Syndrome (PCOS) Genetics
Study
phs000368
-
National Institute of General Medical Sciences (NIGMS) Human Genetic Cell Repository Human Variation Panels including 100 African-Americans (HD100AA), 100 Caucasians (HD100CAU), 100 Han People of Los Angeles (HD100CHI) and 100 Mexican American Community of Los Angeles (HD100MEX)
Study
phs000211
-
Foundation Medicine Adult Cancer Clinical Dataset (FM-AD)
Study
phs001179
-
Direct Transposition of Native DNA for Sensitive Multimodal Single-Molecule Sequencing
Study
phs003511
-
The Effects of Long-Term Heavy Metal Exposure on Transcriptome Landscape in Human Peripheral Blood Cells
Study
phs003657
-
OurHealth - Cardiovascular Disease in South Asians
Study
phs003821
-
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Study
EGAS00001004266
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Study
EGAS00001006904
-
After the completion of CINECA, EUCANCan, and euCanSHare. What's next?
Blog
cineca-eucancan-and-eucanshare-were-concluded-in-june
-
Targeted sequencing data for various human bulk tissues
Dataset
EGAD00001007704
-
CHILD Study Dataset
Dataset
EGAD00001009710
-
13 WGS and 8 TCS data of ENKL patients treated with pembrolizumab.
Dataset
EGAD00001004140
-
Heart Failure Network - Renal Optimization Strategies Evaluation in Acute Heart Failure and Reliable Evaluation of Dyspnea (HFN ROSE-BioLINCC)
Study
phs003589
-
A Platform Study of Combination Immunotherapy for the Neoadjuvant and Adjuvant Treatment of Patients with Surgically Resectable Adenocarcinoma of the Pancreas
Study
phs003002
-
Surgical Treatment for Ischemic Heart Failure (STICH-BioLINCC)
Study
phs003493
-
ALS Compute
Study
phs003184
-
Northwestern NUgene Project: Type 2 Diabetes
Study
phs000237
-
Precision Medicine for ABCA4 Disease: Modifier Alleles
Study
phs002393
-
RNA-Seq of Whole Blood from Patients with Intracranial Aneurysms
Study
phs003072
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
Bacterial Vaginosis, Cervical Immune Cells and HIV Susceptibility
Study
phs002329
-
Profiling Genome-Wide Circulating ncRNAs for the Early Detection of Lung Cancer
Study
phs004166
-
EGA metadata schema
Documentation
submission/metadata/ega-schema
-
Aberrant RNA-splicing (neojunctions) offers a new source for targets, and our neoantigen discovery platform (SNIPP) characterizes a novel class of clonally-expressed splicing-derived neoantigens that elicit a CD8+ T-cell-mediated tumor killing response.
Study
EGAS00001007986
-
RNA sequencing data for primary and recurrent ovarian granulosa cell tumors
Dataset
EGAD00001009108
-
Whole exome and Transcriptome sequencing of treatment-naïve esophageal adenocarcinoma biopsies and matched peripheral blood mononuclear cells
Dataset
EGAD00001010876
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
Impact of Respiratory Virus Infections and Bacterial Microbiome Shifts on Lymphocyte and Respiratory Function in Infants Born Prematurely or Full Term
Study
phs001347
-
Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Study
phs002205
-
Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study - Maternal Glycemia and Birthweight GEI Study
Study
phs000096
-
Broccoli Sprouts Extracts Trial (BEST-COPD-BioLINCC)
Study
phs004022
-
Genome-Wide Association Study of Breast Cancer in the African Diaspora - the ROOT study
Study
phs000383
-
DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing
Study
phs000597
-
The Effect of the Menstrual Cycle on DNA Expression in the Normal Human Breast Epithelium
Study
phs000644
-
NHLBI GO-ESP: Early-Onset Myocardial Infarction Exome Chip (Broad EOMI)
Study
phs000936
-
Rare Genetic Steroid Disease Consortium (GSD) Apparent Mineralocorticoid Excess (AME) Syndrome Natural History Clinical Protocol
Study
phs000603
-
Proteomic Biomarkers of Progressive Fibrosing Interstitial Lung Disease: a Multicentre Cohort Analysis (PF-ILD Proteomics-BioLINCC)
Study
phs003954
-
Exploring high-throughput drug sensitivity testing in neuroblastoma cell lines and patient-derived tumor organoids in the era of precision medicine
Study
EGAS00001007160
-
EGA file encryption types
Documentation
check-encryption-type
-
Genomic Data of Pediatric MDS
Dataset
EGAD00001007856
-
Data upcycling, powered by EGA
Blog
data-upcycling-powered-by-ega
-
A Genome-Wide Association Analysis in Angiotensin-Converting Enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine
Study
phs000438
-
Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer
Study
phs001261
-
The Lung Genomics Research Consortium (LGRC)
Study
phs000624
-
Integrative Single-Cell Analysis of Transcriptome, Epigenome, and Lineage in HIV Latency and Activation
Study
phs002915
-
A Microwell Platform for High-Throughput Longitudinal Phenotyping and Selective Retrieval of Organoids
Study
phs003315
-
Effective screening strategy for deafness using a new-genetation sequencing platform: a consecutive analysis
Study
JGAS000032
-
RNA-seq of high grade serous ovarian tumours
Dataset
EGAD00001009048