-
Whole Genome Sequencing of a Triple Negative Breast Cancer Patient: Matched Primary Tumor, Normal, Metastasis and Xenograft samples
Study
phs000245
-
Genetics of 24 hour urine composition
Study
phs000460
-
Phenotypic and Genotypic Study of Keratoconus
Study
phs003168
-
Out with the Java, in with the Python - new EGA data download client unveiled
Blog
new-ega-data-download-client
-
Cross-Sectional Characterization of Idiopathic Bronchiectasis
Study
phs001279
-
Small cell number RNA-seq (400 cells per sample)
Dataset
EGAD50000001830
-
Paired-end Whole Exome-seq analysis of the 3D evolution of glioma cell populations. Part 2.
Dataset
EGAD00001009496
-
Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk.
Dac
EGAC50000000169
-
Cell-free DNA Methylome Analysis Enables Early Preeclampsia Prediction
Dataset
EGAD00001010159
-
CIDR: Collaborative Study on the Genetics of Alcoholism Case Control Study
Study
phs000125
-
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas
Study
phs001993
-
Study of Controlled Human Malaria Infections to Evaluate Protection After Intravenous or Intramuscular Administration of PfSPZ Vaccine in Malaria-Naive Adults
Study
phs002423
-
PCGP Ph-like ALL
Study
EGAS00001000654
-
Recurrent somatic DICER1 mutations in non-epithelial ovarian tumors
Study
EGAS00001000135
-
Cell-free DNA fragmentation patterns and personalized sequencing reveal circulating tumor DNA in urine and plasma of glioma patients
Study
EGAS00001004355
-
Dataset for liposarcoma-RNA
Dataset
EGAD00001008854
-
Dataset for NSCLC-RNA
Dataset
EGAD00001008846
-
RNA-seq data for study 'Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk.'
Dataset
EGAD50000000333
-
International Age-Related Macular Degeneration Genomics Consortium - Exome Chip Experiment
Study
phs001039
-
Integrative Age-Related Changes in Genome and Epigenome in Human Lung in Relation to Smoking
Study
phs003317
-
Columbia-Yale-Bilkent Study: Genetics Study of Essential Tremor
Study
phs001507
-
High-depth whole genome sequencing of 26 premalignant breast lesions
Study
EGAS50000001559
-
Optimizing Primary Stroke Prevention in Children with Sickle Cell Anemia (STOP II)
Study
phs002386
-
Light at Night and Prostate Cancer in the Health Professionals Follow-Up Study
Study
phs003538
-
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): NIH Digital Health Solutions for COVID-19: Team SAE
Study
phs002534
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – Whole exome sequencing
Study
EGAS00001004832
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – RNA sequencing
Study
EGAS00001004833
-
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
Study
phs001232
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
Quick Guide for data submission
Documentation
submission/quickguide
-
Resuscitation Outcomes Consortium (ROC) Amiodarone, Lidocaine or Neither for Out-Of-Hospital Cardiac Arrest Due to Ventricular Fibrillation or Ventricular Tachycardia (ALPS)(ROC-ALPS-BioLINCC)
Study
phs003784
-
Genetic Aberrations and Subclonal Structure Impact Chronic Lymphocytic Leukemia
Study
phs000922
-
Neoadjuvant combination PD-L1 plus CTLA-4 blockade in patients with cisplatin-ineligible operable urothelial carcinoma
Study
EGAS00001004074
-
HudsonAlpha Long Read Sequencing Data of Individuals with Rare Suspected Genetic Conditions
Study
phs003537
-
Kids First: Whole Genome Sequencing in Recessive Structural Brain Defects
Study
phs002590
-
Blood-based monitoring of relapsed/refractory cHL patients predict responses to PD-1 blockade treatment
Study
EGAS00001005894
-
CNS Embryonal tumors
Dataset
EGAD50000000298
-
IMCISION DNAseq
Dataset
EGAD00001008139
-
Target sequencing of 27 cancer-predisposing genes and 13 renal cell carcinoma-related genes in Japanese renal cell carcinoma patients
Study
JGAS000414
-
Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
-
Virginia PrIMeD Study
Study
phs003609
-
Genetic Analysis of Normal Human Facial Variation
Study
phs000949
-
GA4GH
Documentation
about/projects-and-funders/ga4gh
-
Multi-Site Collaborative Study for Genotype-Phenotype Associations in Alzheimer's disease and Longitudinal follow-up of Genotype-Phenotype Associations in Alzheimer's disease and Neuroimaging component of Genotype-Phenotype Associations in Alzheimer's disease
Study
phs000219
-
Gene Expression and Biomarker Utility in Post-Mortem Samples
Study
phs003546
-
Stratifying and Targeting Pediatric Medulloblastoma through Genomics
Study
EGAS00001000273
-
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Dataset
EGAD00001008314
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010914
-
Epidemiological study comparing rates and risk factors for dementia in African Americans in Indianapolis and Yoruba living in Ibadan, Nigeria
Study
phs000378
-
Diet, Genetic Factors, and the Gut Microbiome in Crohn's Disease
Study
phs000252