-
The Haplotype-Resolved Genome and Epigenome of the Aneuploid HeLa Cancer Cell Line
Study
phs000642
-
INSPIRE - Investigator-initiated Phase 2 Study of Pembrolizumab Immunological Response in Metastatic Solid Tumors
Study
EGAS00001003280
-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
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
-
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
-
San Francisco Bay Area Latina Breast Cancer Study
Study
phs000912
-
DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing
Study
phs000597
-
Nicotine Addiction Genetics and Correlates
Study
phs001299
-
Clinical Proteomic Tumor Analysis Consortium (CPTAC) Proteogenomic Confirmatory Study of Breast, Colon, Lung, and Ovarian Tumors
Study
phs000892
-
Losartan Effects on Emphysema Progression (LEEP-BioLINCC)
Study
phs004313
-
RNA_Seq_in_Patients_with_Primordial_Dwarfism
Study
EGAS00001000283
-
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
-
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
-
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
-
CCDG CVD: VIRGO - Variation in Recover-Role of Gender on Outcomes of Young Acute Myocardial Infarction (AMI) Patients
Study
phs001259
-
Heart Failure Network Oral Iron Repletion Effects on Oxygen Uptake in Heart Failure (HFN IRONOUT-BioLINCC)
Study
phs003557
-
De Novo Mutation Rates at the Single-Mutation Resolution in the Human Genome
Study
phs002391
-
TCR- and BCR-sequencing data for The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Dataset
EGAD00001003985
-
Alzheimer's Disease Sequencing Project (ADSP)
Study
phs000572
-
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