-
Paraganglioma Smart-Seq2 Single Nuclei Sequencing Data
Study
EGAS50000001184
-
Single-cell RNA-seq profiling of patient derived organoids
Study
EGAS50000001025
-
Evaluating potential drug candidates for the treament of Henamgiopericytoma on patient derived cell line models
Study
EGAS50000000027
-
Genomic Data from Patients with Advanced Rare Cancers Treated with Pembrolizumab
Study
EGAS50000001508
-
Transcriptomic Data from Patients with Advanced Rare Cancers Treated with Pembrolizumab
Study
EGAS50000001509
-
ChIP-seq analysis of clear cell renal cell carcinoma
Study
EGAS50000001322
-
Copy number analysis of Diamond-Blackfan Anemia (DBA) using SNP array
Study
EGAS00000000105
-
RNAseq and ATACseq on HGSC lines, pre- and post-treatment with an epigenetic drug
Study
EGAS50000000047
-
Whole exome sequencing data of patients with resectable esophageal adenocarcinoma treated with neoadjuvant atezolizumab and chemoradiation (PERFECT)
Study
EGAS00001006504
-
DCLRE1B/Apollo germline mutations associated with renal cell carcinoma
Study
EGAS50000000216
-
Variables of diversity, clonality, V and J usage and main COVID-19-reactive GLIPH2 frequencies.
Study
EGAS50000000587
-
WES and RNA sequencing of mesothelioma patients from CONFIRM clinical trial
Study
EGAS50000001814
-
Somatic copy number alterations profiling in non-small cell lung cancer and their correlation with clinical efficacy in first-line treatment
Study
EGAS50000001619
-
Neutrophil myeloperoxidase as a functional biomarker for RSV severity: implications for in vitro therapeutic screening
Study
EGAS50000001844
-
Chordoma_Targeted_Sequencing_Study
Study
EGAS00001000280
-
Ribosome_Profiling_of_Macrophages_during_Salmonella_Infection
Study
EGAS00001001285
-
Whole exome sequencing from early stage non-small cell lung cancer patients at MDACC
Study
EGAS00001004026
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
Unraveling_the_genetic_basis_of_a_collagen_migration_defect_in_patients_with_a_combined__platelet_dysfunction_and_reduced_bone_density
Study
EGAS00001000093
-
Exome sequencing of 142 gastric cancer and matched normal from Japanese cohorts (UT)
Study
EGAS00001002891
-
Triple_Negative_Breast_Cancer_Whole_Genome_Validations
Study
EGAS00001000426
-
SPATC1L variants associated with age-related and hereditary hearing loss
Study
EGAS00001003047
-
Osteosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000278
-
Meningioma_Targeted_Sequencing_Study
Study
EGAS00001000282
-
Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
-
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M-mutant pediatric high-grade gliomas
Study
EGAS00001000578
-
16S-based fecal microbiota composition of the Milieu Intérieur Cohort
Study
EGAS00001003419
-
Exome sequencing of stroke cases with good or bad recovery three months after stroke
Study
EGAS00001003463
-
2014 chunnam AML analysis
Study
EGAS00001001082
-
Exome sequencing of 102 gastric cancer and matched normal from Japanese cohorts (YCU)
Study
EGAS00001002892
-
Indonesian RNA-seq data
Study
EGAS00001003671
-
Signals of positive selection in Peruvians from three ecological regions
Study
EGAS00001005692
-
Single-cell RNA-sequencing of CSF cells and PBMCs from individuals with neurological disorders
Study
EGAS00001007954
-
International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results
Study
EGAS00001005110
-
Paired exome and low-coverage genome sequencing of osteosarcoma
Study
EGAS00001005199
-
Genome sequencing of childhood acute leukemia in Iraq
Study
EGAS00001005470
-
Single-cell RNA sequencing dissects gene-environment interactions on gene expression and regulation in immune cells.
Study
EGAS00001005376
-
Whole-Exome Sequences from Imazighen and non-Imazghen from Tunisia
Study
EGAS00001005205
-
Long-read sequencing for cell-free DNA analysis (mouse)
Study
EGAS00001006329
-
WGS of gastric cancer in the Japanese population (81 gastric cancers of NCC)
Study
EGAS00001006051
-
Whole-exome sequencing of paired tumour/blood of 58 T1 stage bladder cancer patients
Study
EGAS00001005765
-
Finding structural variation and functional consequences from the primary leukemia cells (AML) at the single-cell level
Study
EGAS00001004903
-
Plasma whole genome sequencing from patients with stage IV colorectal cancer and microsatellite instability
Study
EGAS00001006377
-
Multiomics analyses of Parkinson's disease midbrains
Study
EGAS00001004966
-
Bone marrow single cell genomics from blood cancer samples
Study
EGAS00001007332
-
Subset of EGAS00001005112 (The INFORM Precision Medicine Study for High-Risk Pediatric Malignancies, 17 exomes) which is used in EGAS00001005243 (Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B)
Dataset
EGAD00001007864
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - WGS data
Study
EGAS50000000657
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - MEGA chip data
Study
EGAS50000000658
-
PCBP1 splicing signature
Study
EGAS50000001859
-
Gut metagenome/FR 2002
Study
EGAS00001005038
-
Framingham Heart Study-Cohort (FHS-Cohort) - BioLINCC
Study
phs003594
-
Genomic Predictors of Combat Stress Vulnerability and Resilience
Study
phs000864
-
Genetics of 24 hour urine composition
Study
phs000460
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Meta-analysis
Study
phs001499
-
Risk Factors for Asymptomatic Diverticulosis
Study
phs003556
-
Field studies of Cryptosporidiosis and Enteropathogens in Bangladesh
Study
phs001665
-
Longitudinal Study of Immune Mediated Disorders After Allogenic Hematopoietic Cell Transplantation (HCT)
Study
phs001331
-
Diabetes Control and Complications Trial (DCCT) and Epidemiology of Diabetes Interventions and Complications Study (EDIC)
Study
phs000086
-
Ischemic stroke in a Swedish case-control study.
Study
EGAS00001000936
-
-
Study
EGAS00001005142
-
Assessment of Health-related Quality of Life in Rare Kidney Stones
Study
phs001770
-
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Red Blood Cell Omics (RBC-Omics) Study
Study
phs001955
-
Direct Transposition of Native DNA for Sensitive Multimodal Single-Molecule Sequencing
Study
phs003511
-
Study of Addiction: Genetics and Environment (SAGE)
Study
phs000092
-
NINDS Inherited Forms of Motor Neuron Disease Study
Study
phs001322
-
RNA-Seq of acute lymphoblastic leukemia in LLAG-0707 study
Dataset
EGAD50000001181
-
Clones derived from early passage tumoroids of colorectal cancer
Dataset
EGAD50000000152
-
Kidney Single Cell Study (2018-08-20)
Dataset
EGAD00001004304
-
Whole-genome sequencing data for inflammatory breast cancer patients
Dataset
EGAD00001005749
-
In this study single cell RNA-Seq data was used to train a deconvolution algorithm. The algorithm was validated on paired bulk RNA-Seq profiles.
Dataset
EGAD00001009688
-
Research Study into The Molecular Genetics of Hereditary Neuropathies
Study
phs001351
-
Cancer Genetic Markers of Susceptibility (CGEMS) Prostate Cancer Genome-Wide Association Study (GWAS) - Primary Scan (Stage 1) - PLCO Screening Trial
Study
phs000207
-
A Prospective Study of Lifestyle, the Gut Microbiome, and Diverticulitis
Study
phs003531
-
A Comprehensive Genomic Study of Pediatric Malignancy
Study
phs001928
-
The Study of Somatic LINE1 Activity in Cancers
Study
phs003888
-
NIBIT-EPI-MESO study samples
Study
EGAS50000001478
-
Mesothelioma Genomics Study - WGS tumour/normal pairs
Study
EGAS00001002299
-
Genome-wide association study of cervical cancer in East Asian populations
Study
EGAS00001003199
-
Queensland Melanoma Genomic Biomarker Study
Study
EGAS00001004619
-
Neuroblastoma and adrenal gland single-cell study
Study
EGAS00001004388
-
Autozygosity pilot - Born in Bradford (2017-05-11)
Dataset
EGAD00001003329
-
Age related Macular Degeneration (AMD) - Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: Association and Sequencing Studies
Study
phs000684
-
Diabetic Retinopathy Genomics Study (DRGen) - Genetic Biomarkers of Diabetic Retinopathy
Study
phs002501
-
MicroRNAs, Hypertension and End Organ Damage in Humans
Study
phs002389
-
Potential Modulatory Role of Osteoprotegerin in Bone Metabolism of Patients with 21-Hydroxylase Deficiency
Study
phs001314
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Study
phs000238
-
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Study
phs000545
-
SNP array analysis of spondylocostal dysostosis patient iPSCs and gene edited isogenic controls
Study
phs001975
-
Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition
Study
phs000873
-
Genomics of Pediatric Renal Medullary Carcinomas
Study
phs001800
-
Genetic Association Studies in the Solomon Islanders
Study
phs000493
-
Single Cell Genomic Analysis of Lymphoma
Study
phs002188
-
DNA Methylation Characterization of Fusion-Positive and Fusion-Negative Rhabdomyosarcoma
Study
phs001970
-
VCRC Genetic Repository One Time DNA Protocol
Study
phs001712
-
Gabriella Miller Kids First Pediatric Research Program in Whole Genome Sequencing of African and Asian Orofacial Clefts Case-Parent Triads
Study
phs001997
-
Genomics of Glomerular Disorders
Study
phs002480
-
Target resequencing of LQTS-related 100 genes in Japanese patients
Study
JGAS000579
-
Clinical Outcomes of 344 Diffuse Large B-Cell Lymphoma patients
Study
EGAS50000001054
-
Single cell RNAseq data of human neurons, Bouwen et al Nat Comm 2025
Study
EGAS50000001369
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00001000245