-
DGCR8 and the six hit, three-step model of schwannomatosis
Study
EGAS00001005665
-
Cell-free DNA and bone marrow samples from myelodysplastic syndromes
Study
EGAS00001005992
-
Transcriptome profiling of three giant cell tumour of bone cell lines
Study
EGAS00001006441
-
Multi-omics analysis defines core genomic alterationsin pheochromocytomas and paragangliomas
Dataset
EGAD00001000986
-
Metabolomic and microbiome profiling reveals personalized risk factors for coronary artery disease
Study
EGAS00001005342
-
The Two Sister Study: A Family-Based Study of Genes and Environment in Young-Onset Breast Cancer
Study
phs000678
-
A Phase 2 Study of Lamivudine in Patients with p53 Mutant Metastatic Colorectal Cancer
Study
phs002833
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Molecular dissection of germline chromothripsis in a developmental context
Study
EGAS00001001896
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
GoDARTS T2D-GENES Exome Sequencing Study is a subset of the ~52,000 Type 2 diabetes exome sequencing project.
Study
EGAS00001002937
-
RA-Map, A multi-omic survey of whole blood and subsets in early rheumatoid arthritis and vaccine study controls
Study
EGAS00001004424
-
Establishment and characterization of an Epstein-Barr virus-positive cell line from a non-keratinizing differentiated primary nasopharyngeal carcinoma
Study
EGAS00001007172
-
Sequencing and analysis of a South Asian-Indian personal genome
Study
EGAS00001000328
-
A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Study
EGAS00001003737
-
Confirmation of a founder effect in a Northern European population (FRL) of a new beta-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))
Study
EGAS00001000980
-
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Study
EGAS00001000643
-
Evolution of a FLT3-TKD mutated subclone at meningeal relapse in acute promyelocytic leukemia (H021)
Study
EGAS00001001848
-
A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients
Study
EGAS00001004491
-
A Machine Learning Tool Integrating Circulating Cell-Free DNA Methylation with Clinical Variables for Non-Invasive Diagnosis of Liver Graft Pathology
Study
EGAS00001007171
-
A Case-Controlled Study for Genotype-Phenotype Associations in Multiple Sclerosis (MS)
Study
phs000171
-
ACTIV-6: COVID-19 Outpatient Randomized Trial to Evaluate Efficacy of Repurposed Medications
Study
phs003941
-
Whole Exome Sequencing of Chronic Lymphocytic Leukemia
Study
phs000435
-
Spit for Science
Study
phs001754
-
Phenotype Risk Scores Identify Patients with Unrecognized Mendelian Disease Patterns
Study
phs001516
-
NIAID Centralized Sequencing Program
Study
phs001899
-
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Study
EGAS00001003950
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
Negligible impact on missing heritability of autoimmune-locus rare coding-region variants
Study
EGAS00001000476
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
-
Non-coding mutations reveal cancer driver cistromes in luminal breast cancer
Study
EGAS00001005235
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Genome-wide association study identifies common variants associated with breast cancer in South African Black women
Study
EGAS00001008032
-
NHLBI TOPMed: Pulmonary Fibrosis Whole Genome Sequencing
Study
phs001607
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000664
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000653
-
Comprehensive analysis of the abnormality of the genes in juvenile myelomonocytic leukemia
Study
JGAS000292
-
Multi-omics analysis of pediatric high-risk neuroblastoma
Study
JGAS000246
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH
Study
EGAS00001002618
-
A Novel APP p.V742L variant in a patient with ischemic small vessel disease enhances FE65 signalling
Study
EGAS50000001283
-
Resistance_to_MAPK_inhibitor_induces_internal_duplication_in_BRAF
Study
EGAS00001001304
-
Whole genome sequencing of Sinonasal hemangiopericytoma and patient derived cell line model
Study
EGAS50000000025
-
Taste Receptor Gene Variants: Body Mass Index (BMI) and Longevity
Study
EGAS00001008403
-
Mutational context and diverse clonal development in early and late bladder cancer
Study
EGAS00001000641
-
Synthetic genotypes and phenotypes of 500.000 individuals
Study
EGAS00001006552
-
RNA-seq on bronchial brushings collected in controlled human exposure to diesel exhaust
Study
EGAS00001006966
-
Longitudinal cfDNA methylome and fragmentome profiles in health
Dataset
EGAD50000001721
-
Genetic data of a monozygotic twin pair discordant for ALS
Dataset
EGAD50000001329