-
Population Genetics Analysis Program: Immunity to Vaccines/Infections - Smallpox Vaccination (NIAID/NIH)
Study
phs001057
-
ABHD11 inhibition drives sterol metabolism to modulate T cell effector function and alleviate autoimmunity
Study
EGAS50000001297
-
RNA expression profiling of neuromuscular diseases and viral diseases
Study
JGAS000064
-
scRNA-seq of patient-derived PDAC organoids and matched CAFs
Study
EGAS00001006661
-
scRNAseq and scATACseq of placebo controlled-trial on MMR non-specific effects
Study
EGAS00001006787
-
Mechanisms of Therapy Driven Clonal Evolution in Oncogenic RAS Mutant Relapsed Acute Lymphoblastic Leukemia
Study
phs001072
-
Altered chromosomal topology drives oncogenic programs in gastrointestinal stromal tumors
Study
phs001906
-
National Heart, Lung and Blood Institute: Regulation of Motile Cilia Assembly in Lung Disease
Study
phs002035
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
-
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Study
EGAS00001002903
-
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis -Part II
Study
EGAS00001003357
-
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Study
EGAS00001001788
-
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
-
Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer
Study
EGAS00001006200
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Study
EGAS00001006692
-
The immunological characterization of expanded tumor-infiltrating lymphocytes in renal cell carcinoma patients
Study
EGAS00001006952
-
Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
-
Phase II Study of Cryoablation and Post-Progression Immune Checkpoint Inhibition in Metastatic Melanoma
Study
phs003579
-
Plasma DNA profile in DNASE1L3 deficiency
Study
EGAS00001004342
-
Whole transcriptome RNA sequencing as comprehensive diagnostic tool for acute myeloid leukemia.
Study
EGAS00001003096
-
Multiple Myeloma Clinical Targeted Sequencing of Patient Samples
Study
phs003908
-
Innate myeloid cell sbuset-specific gene expression patterns in the human colon are altered in Crohn's disease patients
Study
JGAS000127
-
Next-Generation Sequencing of AV Nodal Reentry Tachycardia patients
Study
EGAS00001002745
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Gene Discovery in Autosomal Dominant Focal Segmental Glomerulosclerosis (FSGS)
Study
phs000777
-
Single-cell T-cell receptor sequencing of intraepithelial CD8+ αβ T-cells in celiac disease
Study
EGAS00001004989
-
Post-liver transplant recurrent human hepatocellular carcinoma study (RHCCS)
Study
phs000782
-
Immune Dysregulation in Human Subjects with Heterozygous Germline Mutations in
Study
phs000797
-
Long-read whole genome sequencing as a tool for variant detection in inherited retinal dystrophies
Dataset
EGAD50000001238
-
Whole Transcriptome Sequencing of NXF1 or CRM1 depleted Cell
Study
JGAS000294
-
The origin of post-transplant clonal hematopoiesis can be traced to prenatal development.
Study
EGAS50000000919
-
The_genomic_architecture_of_mesothelioma_
Study
EGAS00001000353
-
Whole genome sequencing of ASD quartet families
Study
EGAS00001001023
-
RNAseq of 76 samples from Uveal Melanoma tumors
Study
EGAS00001002932
-
Functional analysis of GATA2 synonymous mutations
Study
EGAS00001003817
-
Mapping genetic effects on cell type-specific chromatin accessibility using single nucleus ATAC-seq
Study
EGAS00001006184
-
Single-cell RNA-seq of human kidney tumors
Study
EGAS00001006534
-
Dynamics of Genomic and Immune Responses During Primary Immunotherapy Resistance in Mismatch Repair Deficient Tumors
Study
phs002089
-
RNAseq Transcriptomic Analyses of European Ancestry Samples in MGS Dataset
Study
phs001932
-
Circulating Tumor DNA in Intermediate Risk Rhabdomyosarcoma
Study
phs002866
-
The epigenetic landscape controlled by p63 in epidermal development
Study
phs001737
-
Transfer Learning Associates CAFs with EMT and Inflammation in Tumor Cells in Human Tumors and Organoid Co-Culture in Pancreatic Ductal Adenocarcinoma
Study
phs003563
-
Identification and characterization of tertiary lymphoid structures in brain metastases
Study
EGAS50000000563
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma
Study
EGAS00001004076
-
MicroRNA expression in malignant and benign breast tissue – the Norwegian Women and Cancer study
Study
EGAS00001002671
-
Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution.
Study
EGAS00001000840
-
Drugging the catalytically inactive state of RET kinase in RET-rearranged tumors.
Study
EGAS00001002335
-
Integrative sequencing reveals alterations in untreated and castration resistant prostate cancer
Study
EGAS00001000526
-
Splicing patterns in SF3B1 mutated uveal melanoma generate shared immunogenic tumor-specific neo-epitopes
Study
EGAS00001005226
-
Epigenetic profiling of colorectal cancer initiating cells (CC-ICs) to identify bivalently marked genes (H3K4me3 and H3K27me3 ChIP-seq), and investigation of changes in transcriptome following EZH2 inhibition using RNA-seq.
Study
EGAS00001003003
-
Single-cell analysis reveals fibroblast clusters linked to immunotherapy resistance in cancer
Study
EGAS00001004030
-
A mechanistic classification of clinical phenotypes in neuroblastoma
Study
EGAS00001003244
-
Targeting AXL Kinase Uniquely Sensitizes Therapy-Insensitive Leukemic Stem and Progenitor Cells to Venetoclax Treatment in Acute Myeloid Leukemia
Study
EGAS00001004663
-
Single-cell RNA-seq of bronchoalveolar lavage (BAL) fluid in severe COVID-19 and SARS-CoV-2 stimulated classical blood monocytes
Study
EGAS00001004928
-
Characterization and clinical relevance of the genomic alterations defining invasive lobular breast cancer
Dataset
EGAD00001001395
-
InTEAM Consortium - Alcoholic Hepatitis
Study
phs001807
-
Identification of Host Genetic Factors That Are Determinant for the Development of Severe Forms of COVID-19
Study
phs003512
-
Comprehensive genomic profiles of small cell lung cancer
Study
EGAS00001000925
-
tFL with a PMBL GE signature
Study
EGAS00001005870
-
ChIP-Seq of TFEB in LT-HSC
Study
EGAS00001005462
-
cfDNA in health
Study
EGAS50000001209
-
Mutation screening in a large series of Japanese hearing loss patients using massively parallel DNA sequencing analysis.
Study
JGAS000490
-
Investigating transcriptional changes in rapidly differentiated iPSC-derived neurons (i3Ns) harbouring the SNCA A53T mutation +/- RSL3
Study
EGAS50000001536
-
WES Analysis of precancerous lesions in Lynch Syndrome
Study
EGAS50000001546
-
Pre-neoplastic somatic mutations including MYD88L265P in lymphoplasmacytic lymphoma
Study
EGAS00001005656
-
Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
-
COVID-19 GWAS in Japanese
Study
EGAS00001006284
-
cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort
Study
EGAS00001007059
-
Genomic Origins and Admixture in Latinos (GOAL)
Study
phs000750
-
Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer
Study
phs003198
-
Genomic Studies in Charcot-Marie-Tooth Disease
Study
phs003389
-
Impact of Genetic Variation on Response to GO Therapy in COG-AML Trials AAML03P1 and AAML0531
Study
phs003490
-
Analysis of CD20 loss in patients treated with Mosunetuzumab
Study
EGAS50000000151
-
Mortality and risk of progression to adult T-cell leukemia/lymphoma in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis
Study
JGAS000226
-
Recurrent somatic DICER1 mutations in non-epithelial ovarian tumors
Study
EGAS00001000135
-
Exome sequencing in bipolar disorder families
Study
EGAS00001003085
-
Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Study
EGAS00001001575
-
Exome sequencing from cfDNA blood samples. 159 samples at 2x101bp Illumina reads in Fastq format.
Study
EGAS00001006656
-
A New Reference Panel to Boost African American Genotype Imputation
Study
phs001798
-
GnRH Agonist-Induced Ovarian Suppression and Ovarian Steroids in PMDD and Controls
Study
phs001344
-
Early progression to active tuberculosis is a highly heritable trait driven by 3q23 in Peruvians
Study
phs002025
-
Malnutrition and Enteric Disease Network (Mal-ED) Birth Cohort in Brazil
Study
phs003172
-
NHLBI TOPMed - NHGRI CCDG: The GENetics in Atrial Fibrillation (GENAF) Study
Study
phs001547
-
Metatranscriptomic Sequencing of Pulmonary Fluid in Immunocompromised Children
Study
phs001684
-
Transcriptomic Profiling of Peripheral Immune Cells in a Trial of Ruxolitinib with Nivolumab for Anti-PD1 Non-Responsive cHL
Study
phs003601
-
Fragmentomics analyses of urinary cell-free DNA permit multi-urologic cancer detection and reduction in tissue biopsies for prostate cancer
Study
EGAS50000001431
-
Genetics of diffuse large B-cell lymphoma in Japan
Study
JGAS000307
-
HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
-
IKZF5 RNAseq samples for platelets, neutrophils, monocytes and CD4+ T-cells.
Dataset
EGAD00001005107
-
Sequencing_the_exome_of_12_early_sporadic_human_colorectal_cancers__CRC_
Study
EGAS00001000358
-
Targeted sequencing of vascular malformations tissues and paired blood samples
Study
JGAS000325
-
Transcriptome analysis of human iPSC-derived microglia in a novel human 3D cortical tissue model
Dataset
EGAD50000000677
-
1054 Flemish Gut Flora Project (FGFP) samples (16S sequencing, dual index)
Study
EGAS00001003296
-
MDS Sequencing Project_Cancer Cell
Study
EGAS00001001011
-
Melanoma_brain_metastases
Study
EGAS00001002107
-
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Study
EGAS00001005430
-
Identification of Rare Germline Variants in Familial Patients with Non-medullary Thyroid Cancer
Study
phs001758
-
Single cell sequencing reveals the origin and the order of mutation acquisition in T-cell acute lymphoblastic leukemia.
Study
EGAS00001002830
-
Somatic mutations of non-malignant T cells
Study
EGAS50000000237
-
Molecular and Clinical Analyses of PHF6 Mutant Myeloid Neoplasia Provide Clues as to Their Pathogenesis and Therapeutic Targeting
Study
phs003303