-
single cell RNA-seq of small cell lung cancer tumors
Study
EGAS50000001400
-
RNA-seq after drug perturbation of primary lymphoma samples
Dataset
EGAD50000002166
-
RNA Sequencing of Control and Myotonic Dystrophy Type 1 Cells During Myogenic Differentiation
Dataset
EGAD50000001647
-
single cell RNA sequencing and ATAC sequencing, and Whole Genome sequencing of ALS patients
Study
JGAS000852
-
ZFHX4 is necessary for dopaminergic neuron differentiation and controls cell cycle by regulating LIN28A
Dataset
EGAD50000001605
-
3D chromatin contacts of iPSC (controls) and mDAN (differentiated neurons) cells
Study
EGAS50000001578
-
Bulk RNA sequencing of 36 multi-region IPMN–PDAC tumours comprising 160 sequencing runs
Dataset
EGAD50000002215
-
DAC for "Transcriptome analysis of human iPSC-derived microglia in a novel human 3D cortical tissue model"
Dac
EGAC50000000303
-
Yemen_and_Chad_Genotyping
Study
EGAS00001001231
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
HipSci_RNASEQ_BPD
Study
EGAS00001001993
-
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Study
EGAS00001001994
-
HipSci_RNASEQ_Congenital_hyperinsulinia
Study
EGAS00001001988
-
HipSci_RNASEQ_Macular_Dystrophy
Study
EGAS00001001995
-
HipSci_RNASEQ_Alport
Study
EGAS00001001986
-
Breast_cancer_sequential_sampling_study
Study
EGAS00001000300
-
Multiple_Malignancy_Familial_Comparison
Study
EGAS00001000333
-
WTCCC2 Reading and Mathematics (RM) samples
Study
EGAS00001000886
-
Ewings_Sarcoma_Rearrangement_Screen
Study
EGAS00001000362
-
RNAseq_of_patients_with_Ewings_sarcoma
Study
EGAS00001000267
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
Somatic_Variation_Angiosarcoma
Study
EGAS00001002610
-
HipSci_RNASEQ_Kabuki
Study
EGAS00001001989
-
Pre_clinical_evolution_of_haematological_malignancies
Study
EGAS00001002964
-
Exome_sequencing_of_patients_with_Ewings_sarcoma_
Study
EGAS00001000266
-
ERBB2/HER2 transmembrane and juxtamembrane domain mutations in cancer
Study
EGAS00001003213
-
Whole exome sequencing of trio with primary immunodeficiency (IL2RB)
Study
EGAS00001003599
-
HipSci_RNASEQ_Retinitis_Pigmentosa
Study
EGAS00001001996
-
Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
-
Targeted_sequencing_of_cylindroma_patients
Study
EGAS00001002708
-
The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Study
EGAS00001001964
-
Isotype_resolved_sequencing_of_B_cell_receptor__in_health_and_disease
Study
EGAS00001002634
-
Tumor intrinsic and extrinsic mechanisms of response and resistance to blinatumomab in relapsed/refractory acute lymphoblastic leukemia
Study
EGAS00001004027
-
Whole-genome low pass sequencing of 3,514 Sardinian individuals
Study
EGAS00001002212
-
Mexican Biobank Project
Study
EGAS00001005797
-
RNA sequencing of multiple myeloma identifies genes dysregulated by structural variants.
Study
EGAS00001003411
-
Advanced molecular neuropathology to increase diagnostic accuracy in pediatric neurooncology
Study
EGAS00001006680
-
WES on tumor DNA and germline DNA in pediatric cancer
Study
EGAS00001005429
-
Genomic profiling of Rare Tumors
Study
EGAS00001007103
-
Gtag&T single-cell genome and transcriptome data
Study
EGAS00001007043
-
Nasal Polyp RNAsequencing, Skaraborg Sweden
Study
EGAS00001007088
-
Processed RNA-seq data for clinical efficacy and biomarker analysis of neoadjuvant atezolizumab in operable urothelial carcinoma in the ABACUS trial
Dataset
EGAD00001006199
-
Colon Cancer Organoid Cultures and Tumors Whole Exome Sequencing Data
Dataset
EGAD00001005754
-
A living biobank of patient-derived ductal carcinoma in situ Mouse-INtraDuctal xenografts identifies factors associated with risk of invasive progression
Dataset
EGAD00001009336
-
Raw RNA-seq data for clinical efficacy and biomarker analysis of neoadjuvant atezolizumab in operable urothelial carcinoma in the ABACUS trial
Dataset
EGAD00001006205
-
Whole exome sequencing data for Molecular Characterization of ETMRs
Dataset
EGAD00001006210
-
Fine-mapping clustered GWAS hits enhances the identification of disease risk and protective genetic variants
Dataset
EGAD00001006916
-
Genome and transcriptome sequence data from a invasive high-grade serous carcinoma involving tubal mucosa and ovary with serosa patient
Dataset
EGAD00001010971
-
Low Coverage Whole Genome Sequencing from high grade osteosarcoma
Dataset
EGAD00001006540
-
WES of germline, nevi, primary and metastatic Cutaneous Melanoma from patient 009 in CASVAC-0401 trial
Dataset
EGAD00001009083
-
Comprehensive single-cell genome analysis at nucleotide resolution using the PTA Analysis Toolbox
Dataset
EGAD00001011126
-
Epigenetic dysregulation in autism spectrum disorder
Dataset
EGAD00001002725
-
Enhanced Detection of Landmark Minimal Residual Disease in Lung Cancer using Cell-Free DNA Fragmentomics
Dataset
EGAD00001010300
-
A Protein Neddylation Inhibitor MLN4924 Suppresses Patient-Derived Glioblastoma Cells via Inhibition of ERK and AKT Signaling
Dataset
EGAD00001005709
-
Multi-region sequencing of 10 neuroblastoma cases
Dataset
EGAD00001008020
-
Egypt Genome Project - high coverage whole genome sequencing
Dataset
EGAD00001001380
-
Trimmed bam-files from whole genome sequencing data from plasma DNA
Dataset
EGAD00001002254
-
Fastq files used for searching for variants associated with endometriosis at 9p21 region
Dataset
EGAD00001001942
-
Hyperhaploid multiple myeloma
Dataset
EGAD00001004328
-
Egypt Genome Project - low coverage whole genome sequencing
Dataset
EGAD00001001372
-
Clonal expansion of mutated cell population in bladder urothelium
Dataset
EGAD00001003250
-
Genome and transcriptome sequence data from a high grade serous carcinoma of the fallopian tube/ovary/peritoneum patient
Dataset
EGAD00001003702
-
Non-invasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA
Dataset
EGAD00001004989
-
Genomic and clinical data from IMmotion010, a phase 3 randomised clinical trial testing adjuvant atezolizumab versus placebo for patients with renal cell carcinoma at increased risk of recurrence following resection
Dataset
EGAD50000001827
-
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Dataset
EGAD00001005950
-
FFPE
Dataset
EGAD00001006565
-
Single-cell RNA sequencing of erythroid and megakaryocytic acute myeloid leukemia patient cells
Dataset
EGAD00001009865
-
GBM-Space: Spatial Transcriptomic Profiling of Glioblastoma (10x Genomics - Visium)
Dataset
EGAD00001015527
-
Mucociliary Clearance Consortium (MCC) Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age
Study
phs000596
-
Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas
Study
phs001403
-
Study of Osteoporotic Fractures (SOF)
Study
phs000510
-
Analysis of Donor Pancreata Defines the Transcriptomic Signature and Microenvironment of Early Neoplastic Pancreatic Lesions
Study
phs003229
-
Gene mutation and rescue in congenital diaphragmatic hernia
Study
phs000485
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001238
-
Single-cell RNA-Seq of human lymphoma reveals malignant B cell diversity and patterns of T cell immune checkpoint co-expression
Study
phs001378
-
Systems Analysis of the PfSPZ Vaccine in Kenyan Infants
Study
phs002196
-
National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer
Study
phs001935
-
Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Takayasu's Arteritis
Study
phs000589
-
Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
Study
phs000910
-
Kids First Pediatric Research Study in Familial Predisposition to Hematopoietic Malignancies (SJFAMILY-HM)
Study
phs001738
-
NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001345
-
Newborn Screening Translational Research Network (NBSTRN): Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2)
Study
phs002094
-
Hispanic Community Health Study /Study of Latinos (HCHS/SOL)
Study
phs000810
-
Clinical and Molecular Features of Acquired Resistance to Immunotherapy in Non-Small Cell Lung Cancer
Study
phs002834
-
Genetic Investigations of Attention-Deficit/Hyperactivity Disorder
Study
phs003647
-
Cell-Free DNA Genomic and Fragmentomic Features for Early Outcome Prediction in Diffuse Large B-Cell Lymphoma
Study
EGAS50000000412
-
Phase 1/2 Study of the Indoleamine 2,3-Dioxygenase 1 Inhibitor Linrodostat Mesylate Combined With Nivolumab or Nivolumab and Ipilimumab in Advanced Solid Tumors or Hematologic Malignancies
Study
EGAS50000000710
-
Investigating Delayed-Onset Drug Hypersensitivity Reactions Prospectively
Study
phs003344
-
Repeat expansions with small TTTCA insertions in MARCHF6 cause Familial Adult Myoclonus without Epilepsy
Study
EGAS50000000570
-
HeLa Cell Genome Sequencing Studies
Study
phs000640
-
Cellular Profiling Identifies Targetable T Cell Phenotypes in Lymphocytic Variant Hypereosinophilic Syndrome
Study
phs004041
-
Research in Adaptive Interests, Skills, and Environment
Study
phs003982
-
IDH-wildtype untreated human glioblastoma samples (GB-UK cohort), published in Noorani & Haughey et al 2025.
Study
EGAS00001008126
-
Mortality and risk of progression to adult T-cell leukemia/lymphoma in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis
Study
JGAS000226
-
Indonesian Genome Diversity Project
Study
EGAS00001003054
-
The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia
Study
EGAS00001004212
-
Molecular subtypes of pancreatic neuroendocrine tumors mutated in MEN1/DAXX/ ATRX explain biological variability
Study
EGAS00001008272
-
Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer Genes in Endometrial Cancer
Study
EGAS00001000318
-
Tracking the evolution of Therapy-Related Myeloid Neoplasms using chemotherapy signatures
Study
EGAS00001006903