-
Illumina HumanOmniExpress genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study.
Study
EGAS00001000996
-
Field Studies of Human Immunity to Amebiasis in Bangladesh (NIH Birth Cohort) and Exploration of the Biologic Basis for Underperformance of Oral Polio and Rotavirus Vaccines in Bangladesh (PROVIDE)
Study
phs001475
-
Multiomic characterization of clonotypic B cells
Dataset
EGAD50000002162
-
Glioblastoma stem cell lines RNA-seq (Guilhamon et al.)
Dataset
EGAD00001006813
-
Whole blood RNA-sequencing of covid-19 patients and healthy controls
Dataset
EGAD00001007776
-
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
Dataset
EGAD00001007794
-
Cryopreservation of human cancers conserves tumour heterogeneity for single-cell multi-omics analysis
Dataset
EGAD00001007030
-
RNA Expression in Diverse Donor Derived Dermal Fibroblasts Correlates with Reprogramming to Pluripotency
Study
phs002341
-
The Role of E2F4 in Controlling Resistance to Irinotecan (CPT-11) in Human Colon Cancer
Study
phs003560
-
Weighing Risks and Benefits of Laparoscopic Anti-Reflux Surgery in Patients With Idiopathic Pulmonary Fibrosis (WRAP-IPF-BioLINCC)
Study
phs003968
-
Transcriptomic analysis of liver CD8+ T cells
Study
EGAS00001006885
-
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Study
phs000564
-
Biomarkers in Transplant Recipients
Study
phs000960
-
Indexing Genes Impacted by Copy Number Variation in Developmental Disorders
Study
phs001154
-
Genome Wide Association for Asthma and Lung Function
Study
phs000355
-
Whole Exome Sequencing of DNA from Pre-and Post-Chemotherapy Needle Biopsies of Triple Negative and Inflammatory Breast Cancers Enrolled in the S0800 Trial
Study
phs001883
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Meta-analysis
Study
phs001499
-
The Genetics of Type 2 Diabetes Consortium (GoT2D): Low-Pass Sequencing and High-Density SNP Genotyping for Type 2 Diabetes
Study
phs000840
-
Trisomy 21 Dosage Compensation Map (T21DoCoMap)
Study
phs002397
-
The Genomic and Transcriptomic Landscape of a HeLa Cell Line
Study
phs000643
-
Field studies of Cryptosporidiosis and Enteropathogens in Bangladesh
Study
phs001665
-
NIPT samples for systematic evaluation of BinDel, a software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Dataset
EGAD00001009512
-
GWAS Results from Danjou et al, Nature Genetics 2015
Study
EGAS00001003645
-
RNA sequencing data of 257 samples from the CORALLEEN trial
Dataset
EGAD00001010121
-
TRACERx100 metastatic samples
Dataset
EGAD00001003301
-
Long-Term Oxygen Treatment Trial (LOTT-BioLINCC)
Study
phs003933
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415
-
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Study
phs001037
-
CIDR, NCI, NIDA Sequencing of Targeted Genomic Regions Associated with Smoking
Study
phs000813
-
Somatic Genome Dynamics of Barrett's Esophagus Patients with Non-Cancer and Cancer Outcomes
Study
phs001912
-
SLCO1B1 Variants and Methotrexate Clearance
Study
phs000426
-
Age related Macular Degeneration (AMD)-- Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: A Joint Genome Wide Association Study
Study
phs000182
-
Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses
Study
phs002031
-
Genomic Characterization of Duke Melanoma Brain Metastases
Study
phs003009
-
Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702
-
Healthy_ageing_thymus
Study
EGAS00001004311
-
TCR- and BCR-sequencing data for The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Dataset
EGAD00001003985
-
Bladder Cancer Organoids as a Functional System to Model Different Disease Stages and Therapy Response
Study
phs003149
-
NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate
Study
phs001359
-
Exome Sequencing to Identify Medically Relevant Associations in Finnish Sub-Isolate Samples from the FINRISK Cohort
Study
phs000756
-
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Study
phs000801
-
Aspirin and Inflammation: Mutations, Genes, Pathways and Prevention in Barrett's Esophagus
Study
phs001654
-
A Population Genomics Study Using a Disease-Targeted Cell model: Integration of
Study
phs000225
-
Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Study
phs000413
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Study
phs000422
-
Ghana Prostate Study
Study
phs000838
-
AC-ICAM: An Atlas and Compass of Immune-CAncer-Microbiome Interactions in Colon Cancer
Study
phs002978
-
NINDS Deep Sequencing for the Detection of Viral Sequences in Primary Progressive Multiple Sclerosis Brains
Study
phs000715
-
Glial Cell Line-Derived Neurotrophic Factor (GDNF) Polymorphisms and Anxiety, Depression
Study
phs000713
-
Genomic Landscape of Multiple Myeloma and of its Precursor Conditions, and its Clinical Implications
Study
phs003846