-
Mayo Clinic Adult Diffuse Glioma Illumina OncoArray SNP Data
Study
phs003041
-
Human Epilepsy Genetics: Mosaic Mutations in Focal Epilepsy
Study
phs004124
-
Isala Citizen Science Project: Cross-sectional branch
Study
EGAS00001006934
-
Single-cell roadmap of immune cell responses in chronic myeloid leukemia
Study
EGAS00001005044
-
Whole Genome Sequencing of Bilateral Cleft Lip and Palate Families from Africa: CIDR
Study
phs002623
-
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Study
JGAS000073
-
Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
Study
JGAS000107
-
RNA-seq analysis of megakaryocytes and granulocytes in Quebec platelet disorder
Study
EGAS00001001840
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Genetic Variants Influence on the Placenta Regulatory Landscape
Study
phs001717
-
Searching for rare/low frequency variants in rheumatoid arthritis by exome sequencing
Study
JGAS000035
-
Integrative_Oncogenomics_of_multiple_myeloma
Study
EGAS00001000243
-
scRNA-seq data of BALF and blood cells from COPD and control
Study
EGAS00001004369
-
Mapping genetic variants that underlie gene regulation in intestinal cell types to identify novel, validated, Crohn’s disease drug targets
Study
EGAS00001003647
-
GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
Study
phs001074
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Gabriella Miller Kids First Pediatric Research Program of the Pediatric Cardiac Genetics Consortium (PCGC)
Study
phs001138
-
Atezolizumab and Bevacizumab in Treating Patients With Rare Solid Tumors
Study
phs003845
-
Genomic features of renal cell carcinoma developed in end-stage renal disease and dialysis
Study
JGAS000533
-
Genomic profiling of matched well differentiated and de-differentiated liposarcoma.
Study
EGAS00001002807
-
Targeted sequencing of genomic regions of interest in depression and obesity
Study
EGAS50000000330
-
Spatial heterogeneity, stromal phenotypes, and therapeutic vulnerabilities in colorectal cancer peritoneal metastasis
Study
EGAS50000000813
-
GOSH_Tumour_Embryology_Paediatric_Behjati_RNA_Managed_Access
Study
EGAS00001006737
-
Clonal Evolution and Heterogeneity of Osimertinib Acquired Resistance Mechanisms in EGFR Mutant Lung Cancer
Study
phs002001
-
Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Study
EGAS00001000737
-
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
-
EASI-Genomics GM21886 Cell Line High Molecular Weight DNA Sequencing
Study
phs003958
-
Skin Microbiome of Monogenic Skin Disorder
Study
phs003799
-
Bulk and RIP-seq transcriptome datasets from skin fibroblasts in PTBP1- and PTBP2-related disorders
Study
EGAS50000001210
-
ecDNA copy number heterogeneity
Study
EGAS50000000509
-
RODAM cohort
Study
EGAS50000000805
-
EXCEED Study
Study
EGAS00001003499
-
Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF
Study
EGAS00001005863
-
Rearrangements of the MAST Kinase and Notch Gene Families in Breast Cancer
Study
phs000513
-
GWA Study of Oral Cavity, Pharynx and Larynx Cancers in European, and North and South American Populations - CIDR
Study
phs002503
-
Separation, characterization, and identification of individuals from multi-person blood mixtures with single cell ATAC-seq
Study
EGAS00001007380
-
Genomic characterization of a patient with AGS and CdLS transcriptomic comparison of his monocytes against healthy and disease control samples
Study
EGAS00001007829
-
TIGER-LC High-Throughput Sequencing
Study
phs001199
-
Gene expression in brain (Schizophrenia) study
Study
EGAS00001004199
-
Smoking and the Vaginal Microbiome
Study
phs001386
-
Germline Genetics of Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML)
Study
phs002962
-
Nurminen et al ("GP2Men") Study Primary and Metastatic Prostate Cancer Whole Genome Sequence Data
Dataset
EGAD50000000005
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC)
Study
phs000571
-
Genetic and epigenetic analysis of individuals with porokeratosis
Study
JGAS000684
-
Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS)
Study
phs001119
-
NHLBI TOPMed: SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS)
Study
phs001927
-
Lactobacillus rhamnosus GG ATCC (LGG) as an immune adjuvant for influenza vaccination in the elderly
Study
phs000981
-
Human inflammatory cardiomyopathies following SARS-CoV2 infection and COVID-19 vaccination
Study
EGAS50000000769
-
Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma
Study
EGAS00001003438
-
glioblastoma and glioblastoma stem cells (GSCs), RNA-seq and WGS
Study
EGAS00001004395
-
Environmental Influences on Child Health Outcomes (ECHO) - PATHWAYS - Conditions Affecting Neurocognitive Development and Learning in Early Childhood (CANDLE)
Study
phs003619
-
Environmental Influences on Child Health Outcomes (ECHO) - PATHWAYS - Global Alliance to Prevent Prematurity and Stillbirth (GAPPS)
Study
phs003620
-
Extraembryonic tissue and cytotrophoblast epigenome mapping
Dataset
EGAD00001006066
-
Spectrum and significance of MYC and BCL2 mutations in DLBCL
Study
EGAS00001002206
-
scD&D Multiome of GATA1 regulatory network dynamics during erythropoiesis
Study
EGAS50000001606
-
Mutational_burden_in_oesophagus__nanoseq_
Study
EGAS00001007695
-
single cell data from HPV-positive head and neck cancer patients receiving induction CTLA-4 and PD-1 immune checkpoint blockade
Study
EGAS50000000335
-
Whole-Exome Sequencing Plasma Control Samples for Benchmarking
Study
EGAS50000000565
-
NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)
Study
phs001467
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Strong Heart Study (SHS) and Strong Heart Family Study (SHFS)
Study
phs000580
-
Single Cell Analysis Program - Transcriptome (SCAP-T)
Study
phs000833
-
Molecular subsets in renal cancer determine outcome to checkpoint and angiogenesis blockade
Study
EGAS00001004353
-
MethCORR: DNA Methylation-based Characterization, Classification and Prognostication of Colorectal Cancer using Archival Formalin-fixed, Paraffin-embedded Tissue
Study
EGAS00001004293
-
After the completion of CINECA, EUCANCan, and euCanSHare. What's next?
Blog
cineca-eucancan-and-eucanshare-were-concluded-in-june
-
Kids First: Genomic Etiologies of CHARGE Syndrome, Related Conditions and Structural Anomalies
Study
phs002592
-
Resolution and methylation patterns of supernumerary marker chromosomes
Study
EGAS50000001466
-
Amsterdam UMC Head and Neck Cancer Biology and Immunology
Dac
EGAC50000000350
-
Intervention with Micronutrients and Long-Term Impact in Brazil-RECODISA
Study
phs003174
-
Whole Genome, Exome, Transcriptome and Validation Sequencing of an Acute Lymphoblastic Leukemia
Study
phs001066
-
Genomics and Methylation of Neuroendocrine Prostate Cancer from cfDNA (Cornell/Trento 2019)
Study
phs001752
-
Healthy and FPD Bone Marrow Single Cell Sequencing
Study
phs003508
-
Geographical structure and differential natural selection among North European populations
Study
EGAS00000000033
-
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
-
A Genome Wide Scan of Lung Cancer and Smoking
Study
phs000093
-
Kids First Pediatric Research Study in Familial Predisposition to Hematopoietic Malignancies (SJFAMILY-HM)
Study
phs001738
-
Integration of Genomics and Transcriptomics in unselected Twins and in Major Depression
Study
phs000486
-
NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Study
phs001515
-
NHLBI GO-ESP: Family Studies (Familial Atrial Fibrillation)
Study
phs000362
-
Cancer Moonshot Biobank
Study
phs002192
-
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Digital Health Solutions for COVID-19: COVID Community Action and Research Engagement (COVID-CARE)
Study
phs002533
-
Minnesota Center for Twin and Family Research (MCTFR) Genome-Wide Association Study of Behavioral Disinhibition
Study
phs000620
-
OncoArray: Oral and Pharynx Cancer
Study
phs001202
-
Combined PDCD1, BRAF and MAP2K7 Inhibition in BRAFV600E Colorectal Cancer: A Phase 2 Trial
Study
phs003178
-
Translational analyses from a phase II study of pembrolizumab and epigenetic modification with azacitidine in platinum-resistant epithelial ovarian cancer
Study
EGAS50000001165
-
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Study
EGAS00001004886
-
The genomic and radiomic complexity of multifocal prostate cancer
Study
EGAS00001002767
-
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Study
EGAS00001006819
-
160 WES and 25 WGS for HBV related HCC, and 15 WES for ICC belongs LICA-CN.
Study
EGAS00001002331
-
The Longevity Genes Project
Study
phs000584
-
Sensitivity to the Subjective Effects of Amphetamine
Study
phs000832
-
The Oral Microbiome and Head and Neck Cancer
Study
phs004018
-
The characterization of gene expression pattern of anticancer agent-resistant cancer stem cells using RNA sequencing analysis.
Study
JGAS000350
-
National Institute on Alcohol Abuse and Alcoholism (NIAAA) Postmortem Prefrontal Cortex eQTL and mQTL Study
Study
phs001981
-
The preterm infant microbiome: biological, behavioral and health outcomes at 2 and 4 years of age
Study
phs001578
-
Esophageal Squamous Cell Carcinoma Precursor Study
Study
phs002814
-
Single_cell_characterization_of_T_cell_lymphoma_
Study
EGAS00001005750
-
Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study - Maternal Glycemia and Birthweight GEI Study
Study
phs000096
-
Drug Signatures for Prediction and Mitigation of Toxicity
Study
phs002088
-
Childhood Cancer Data Initiative (CCDI): Molecular Characterization across Pediatric Brain Tumors and Other Solid and Hematologic Malignancies for Research, Diagnostic, and Precision Medicine
Study
phs002517
-
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
Study
phs001232
-
Collaborative Study of Genes, Nutrients and Metabolites (CSGNM)
Study
phs000789