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A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
Nurminen et al ("GP2Men") Study Primary and Metastatic Prostate Cancer Whole Genome Sequence Data
Study
EGAS50000000005
-
DAC Admixture histories of São Tomé e Príncipe
Dac
EGAC50000000437
-
SUM-seq data for spontaneously differentiated iPSCs to EBs
Dataset
EGAD50000001589
-
Single-cell RNA sequencing of control and Notch inhibitor treated HCC PDX model
Dataset
EGAD50000000738
-
The effect of freezing delay of cell-type specific transcriptome responses in human brain via snRNA-seq
Dataset
EGAD00001008541
-
Targeted Myeloid DNA-Panelsequencing, DKFZ
Dataset
EGAD00001008501
-
Mechanisms of patient response to Dabrafenib in Melanoma
Dataset
EGAD00001001375
-
Tagged-amplicon deep sequencing
Dataset
EGAD00001011058
-
Comprehensive cancer predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes
Dataset
EGAD00001004088
-
Drug development for pediatric cancers: the importance of patient' s genomic data re-use
Blog
drug-development-for-pediatric-cancers
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The African American Breast Cancer Epidemiology and Risk (AMBER) Consortium Study
Study
phs000669
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
PREDICT-HD Huntington Disease Study
Study
phs000222
-
NIMH Human Middle Temporal Gyrus (MTG) Cell Types
Study
phs001790
-
Children's Hospital of Philadelphia (CHOP) Control Copy Number Variation (CNV) Study
Study
phs000199
-
Single-cell RNA-seq of rheumatoid arthritis synovial tissue using low-cost microfluidic instrumentation
Study
phs001529
-
NHLBI TOPMed: Genome-Wide Association Study of Adiposity in Samoans
Study
phs000972
-
The Bangladesh Environmental Enteric Dysfunction (BEED) Study
Study
phs001891
-
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
-
Illumina HumanOmniExpress genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study.
Study
EGAS00001000996
-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
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
-
TRACERx100 metastatic samples
Dataset
EGAD00001003301
-
RNA sequencing data of 257 samples from the CORALLEEN trial
Dataset
EGAD00001010121
-
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
-
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
-
Genomic Landscape of Multiple Myeloma and of its Precursor Conditions, and its Clinical Implications
Study
phs003846
-
A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Study
EGAS00001002975
-
Post_Mortem_Tissue_COVID19_RNA
Study
EGAS00001004442
-
Post_Mortem_Tissue_COVID19_spatial
Study
EGAS00001004441
-
Single cell RNAseq data of human neurons, Bouwen et al Nat Comm 2025
Study
EGAS50000001369
-
Molecular characterization of NASH-HCC
Dataset
EGAD00001007524
-
CRUK-ICGC Prostate DNA Methylation Sequencing Dataset (Prostatectomy Batches 1-6)
Dataset
EGAD00001010184
-
Women's Health Initiative Clinical Trial and Observational Study - Imaging
Study
phs003824
-
Prevention and Early Treatment of Acute Lung Injury Network - Vitamin D to Improve Outcomes by Leveraging Early Treatment (PETAL VIOLET-BioLINCC)
Study
phs003879
-
Atezolizumab Plus Personalized Neoantigen Vaccination in Patients with Urothelial Cancer: a Phase 1 Trial
Study
phs003922
-
RNA-Seq in Patients with Primordial Dwarfism
Dataset
EGAD00001000640
-
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
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Coronary Artery Risk Development in Young Adults (CARDIA)
Study
phs000236
-
Phenotypic and Genotypic Study of Keratoconus
Study
phs003168
-
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Study
phs001831
-
Heart Failure Network - Effectiveness of Ultrafiltration in Treating People with Acute Decompensated Heart Failure and Cardiorenal Syndrome (HFN CARRESS - BioLINCC)
Study
phs003510
-
Light at Night and Prostate Cancer in the Health Professionals Follow-Up Study
Study
phs003538
-
Parallel CRISPR Editing of Familial ALS Mutations
Study
phs002440
-
Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
-
WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
-
Highlights from 2025: Our top 10 requested studies
Blog
top-10-studies-2025
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NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Siblings with Ischemic Stroke Study, SWISS)
Study
phs000327