-
RNA-seq of longitudinal human blood and nose swab samples from a controlled human infection experiment with SARS-CoV-2 virus
Dataset
EGAD50000000942
-
scRNA-seq of HSPC treated with gemcitabine and carboplatin
Dataset
EGAD00001006080
-
Whole exome sequencing of a representative cohort of AML
Dataset
EGAD00001007580
-
Somatic mutation rates scale with lifespan across mammals
Dataset
EGAD00001008032
-
A Study to Assess the Cardiovascular, Cognitive, and Subjective Effects of Atomoxetine in Combination with Intravenous Methamphetamine
Study
phs001195
-
A Randomized Trial of Combined PD-L1 and CTLA-4 Inhibition with Targeted Low-Dose or Hypofractionated Radiation for Patients with Metastatic Colorectal Cancer
Study
phs003294
-
Durvalumab Plus Tremelimumab Alone or in Combination with Low-Dose or Hypofractionated Radiotherapy in Metastatic Non-Small-Cell Lung Cancer Refractory to Previous PD(L)-1 Therapy: an Open-Label, Multicentre, Randomised, Phase 2 Trial
Study
phs003295
-
Whole Transcriptome Sequencing of Resectable Stage III/IV Melanoma Evaluated After Starting Hu14.18-IL2 Predicts Outcome
Study
phs001947
-
Longitudinal Study of Immune Mediated Disorders After Allogenic Hematopoietic Cell Transplantation (HCT)
Study
phs001331
-
GEnetics of Nephropathy - an International Effort (GENIE) GWAS of Diabetic Nephropathy in the UK GoKinD and All-Ireland Cohorts
Study
phs000389
-
Mechanism of Action of Vitamin E in NAFLD
Study
phs001930
-
PROGRESS/ELEMENT DNA Methylation Study
Study
phs002754
-
Diabetes Control and Complications Trial (DCCT) and Epidemiology of Diabetes Interventions and Complications Study (EDIC)
Study
phs000086
-
Resistance to Checkpoint Blockade Therapy Through Inactivation of Antigen Presentation
Study
phs001427
-
Gene mutation and rescue in congenital diaphragmatic hernia
Study
phs000485
-
Human Gene Expression Patterns Associated with Experimental P. falciparum Infection
Study
phs001346
-
A Polygenic Score for Acute Vaso-Occlusive Pain in Pediatric Sickle Cell Disease
Study
phs002470
-
The Role of Germline Mutation and Parental Age in Autism Spectrum Disorders
Study
phs001164
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Study
phs000422
-
Genetic Analysis of Parkinson's Disease
Study
phs001004
-
Ghana Prostate Study
Study
phs000838
-
Genotyping NIGMS CEPH Samples from the United States, Venezuela, and France
Study
phs000268
-
Center Common Disease Genomics [CCDG] - Cardiovascular: Partners Biobank
Study
phs002018
-
Newborn Screening Translational Research Network (NBSTRN): Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2)
Study
phs002094
-
Sudden Death in the Young Case Registry
Study
phs003221