-
Evolutionary dynamics of residual disease in human glioblastoma
Study
EGAS00001003043
-
Exome sequencing in bipolar disorder families
Study
EGAS00001003085
-
Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Study
EGAS00001001244
-
UK10K NEURO IMGSAC
Study
EGAS00001000120
-
Targeted Gene Panel for 171 PTCLs
Study
EGAS00001002740
-
Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma
Study
EGAS00001000622
-
Whole exome sequencing of small cell neuroendocrine cancer of the cervix
Study
EGAS00001003142
-
Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing
Study
EGAS00001000962
-
We evaluate the potential for routine WGS using ONT by sequencing the well-characterised reference sample NA12878 and the genome of an individual with ataxia-pancytopenia syndrome accompanied by severe immune dysregulation.
Study
EGAS00001003469
-
Post_Mortem_Tissue_COVID19_RNA
Study
EGAS00001004442
-
Post_Mortem_Tissue_COVID19_spatial
Study
EGAS00001004441
-
Tumor-specific expression of let-7i and miR-192 is associated with resistance to cisplatin-based chemoradiotherapy in patients with larynx and hypopharynx cancer
Study
EGAS00001004001
-
The clinical utility of genomics in childhood cancer extends beyond targetable mutations
Study
EGAS00001006034
-
Genetic immune escape landscape in primary and metastatic cancer
Study
EGAS00001006123
-
Long-term temporal stability of peripheral blood DNA methylation alterations in patients with inflammatory bowel disease.
Study
EGAS00001006501
-
T-cell receptor sequencing of tumor-infiltrating lymphocytes (TIL) in breast cancer
Study
EGAS00001007125
-
IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
-
Multi-omic analysis of Down Syndrome in thyroid
Study
EGAS00001007677
-
Profiled samples in the study "Chromatin activation profiling of stereotyped chronic lymphocytic leukemias reveals a subset #8 specific signature"
Dac
EGAC00001002787
-
Clinical and genetic analysis of a rare syndrome associated with neoteny
Dataset
EGAD00001003593
-
Data for paper Mold, Weissman et al. 'Clonally heritable gene expression imparts a layer of diversity within cell types'
Dac
EGAC50000000102
-
The Sys4MS cohort: a prospective cohort of patients with Multiple Sclerosis and omics
Study
EGAS00001007145
-
Targeting the Epichaperome As an Effective Precision Medicine Approach in a Novel PML-SYK Fusion Acute Myeloid Leukemia
Study
EGAS00001004992
-
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Study
EGAS00001004430
-
Anti-Cancer Therapies Induce Mutations in Adult Stem Cells in a Tissue-Specific Manner
Study
EGAS00001006042
-
ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution
Study
EGAS00001006268
-
Case Report: early contribution of germline and nevi genetic alterations to a rapidly-progressing Cutaneous Melanoma Patient
Study
EGAS00001006459
-
Elevated cfDNA after exercise is derived primarily from mature polymorphonuclear neutrophils, with a minor contribution of cardiomyocytes
Study
EGAS00001007157
-
DKFZ-HIPO DACO for "Patient-derived tumoroids from CIC::DUX4 rearranged sarcoma identify MCL1 as a therapeutic target"
Dac
EGAC00001003559
-
Data Access Committee for Patient-derived tumoroids from CIC::DUX4 rearranged sarcoma identify MCL1 as a therapeutic target
Dac
EGAC00001003558
-
Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study
Study
phs001307
-
REDS-IV-P Epidemiology, Surveillance and Preparedness of the Novel SARS-CoV-2 Epidemic (RESPONSE)
Study
phs003578
-
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
-
Public Access Defibrillation Community Trial (PAD)(PAD-BioLINCC)
Study
phs003858
-
Lipid Research Clinics - Prevalence Study (LRC-PS-BioLINCC)
Study
phs003995
-
Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT-BioLINCC)
Study
phs004021
-
HeartShare - Extant Datasets - Harmonized Clinical Trials Collection
Study
phs003989
-
Study of 5'UTR Mutations in Prostate Cancer
Study
phs001825
-
NHLBI TOPMed: The Genetics and Epidemiology of Asthma in Barbados
Study
phs001143
-
RNA Splicing Dysregulation in the Pathogenesis of Chronic Lymphocytic Leukemia
Study
phs003191
-
NIDDK IBD Genetics Consortium Repository Exome Chip
Study
phs001723
-
Whole Exome and Whole Genome Profiling as well Genome-Wide Methylation Profiling from Early to Advanced Chronic Lymphocytic leukemia (CLL), Genome-Wide Methylation Profiling in Monoclonal B Cell Lymphocytosis (MBL)
Study
phs001431
-
Integrated Genomic Analyses of Cutaneous T Cell Lymphomas Reveal the Molecular Bases for Disease Heterogeneity
Study
phs002456
-
Inhibition of CDK4/6 Promotes CD8 T Cell Memory
Study
phs002448
-
Screening Cases of Isolated Dystonia for Variants in CIZ1
Study
phs001455
-
Genentech whole genome and transcriptome sequencing of four hepatocellular carcinoma patients
Study
phs000384
-
Genomics of Pediatric Renal Medullary Carcinomas
Study
phs001800
-
Genetic Association Studies in the Solomon Islanders
Study
phs000493
-
Hyperdiploid Acute Lymphoblastic Leukemia RNA-Seq
Study
phs000522
-
Whole-Exome Sequencing and Targeted DNA Sequencing of Matched Ocular Melanocytosis and Uveal Melanoma
Study
phs001835
-
GWAS for Membranous Nephropathy
Study
phs001984
-
Dana-Farber Cancer Institute (DFCI) Wu Lab/Avicenne CLL RNA-Seq Study
Study
phs002335
-
Epidemiologic Architecture for Genes Linked to Environment (EAGLE) MetaboChip Study
Study
phs002767
-
Germline Whole-Exome Sequencing of Lung Cancer in EAGLE
Study
phs002496
-
Natural Genetic Variation in the Human Genome
Study
phs002463
-
Center for Common Disease Genomics (CCDG) - Cardiovascular: BioImage Cohort
Study
phs002325
-
Multi-Modal Single-Cell and Whole-Genome Sequencing of Small, Frozen Clinical Specimens
Study
phs003097
-
NHLBI TOPMed - NHGRI CCDG: The Vanderbilt University BioVU Atrial Fibrillation Genetics Study
Study
phs001624
-
Cross-site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms of CIMAC-CIDC Network
Study
phs002295
-
Multicenter International Cross-Sectional Evaluation of Pulmonary Alveolar Proteinosis (MICEPAP) Trial
Study
phs001309
-
Whole Exome Sequencing for Familial Intracranial Aneurysm (FIA I-II) Study
Study
phs000636
-
DAC for Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Dac
EGAC50000000332
-
AYA glioma NGS
Study
EGAS50000000383
-
DirectHRD Enables Sensitive Scar-Based Classification of Homologous Recombination Deficiency (HRD)
Study
phs003760
-
Genomic Changes in Breast Cancer Among Chinese Women in Hong Kong
Study
phs001870
-
DNA Repair Capacity for Lung Disease Risk Assessment
Study
phs004063
-
Establishment and genomic analysis of mixed phenotypic acute leukemia cell lines
Study
JGAS000721
-
Target resequencing of LQTS-related 100 genes in Japanese patients
Study
JGAS000579
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00001000245
-
Prostate Cancer and Normal Adjacent Prostate RNA-seq samples, NGS-ProToCol
Study
EGAS00001002816
-
H3Africa - Respiratory Microbiota of African Children
Study
EGAS00001004401
-
Single-cell profiling of the leukemic and non-leukemic immune cell compartments in CD8+ T-cell Large Granular Lymphocytic Leukemia
Study
EGAS00001005297
-
RNA-seq study of longitudinal blood cell samples from children at risk of type 1 diabetes
Study
EGAS00001004071
-
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathie
Study
EGAS00001002506
-
Low_coverage_whole_genome_sequencing_of_samples_from_the__Cretan_Greek_isolate_collection_HELIC_MANOLIS
Study
EGAS00001000392
-
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Study
EGAS00001001501
-
PCa-LINES
Study
EGAS00001004613
-
Genome Asia 100K Project
Study
EGAS00001002921
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
EGAS00001007027
-
'IL-17A-Producing ILC3s and Duodenal Adenoma in FAP'
Study
EGAS00001007347
-
WES dataset of 20 pre-post paired neoadjuvant chemotherapy treated breast cancer samples
Dataset
EGAD00001008442
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Dataset
EGAD00001007872
-
Exome sequencing of UK Birth Cohorts - Millennium Cohort Study
Dataset
EGAD00001015372
-
Exome sequencing of UK Birth Cohorts - Avon Longitudinal Study of Parents and Children
Dataset
EGAD00001015371
-
Peripheral blood DNA methylation of Crohn's disease patients starting treatment with adalimumab, vedolizumab or ustekinumab
Study
EGAS00001007532
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Dac
EGAC00001002145
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Dac
EGAC00001002151
-
methylomics
Dataset
EGAD00010001660
-
Time series analysis of neoadjuvant chemotherapy and bevacizumab treated breast carcinomas reveals a systemic shift in genomic aberrations
Study
EGAS00001003287
-
Whole Exome Sequencing of Schizophrenia cases and controls performed at the Broad Institute on a cohort from Bristol, UK
Study
EGAS00001006274
-
Whole-genome sequencing of a census-based elderly cohort of Brazilians
Study
EGAS00001005052
-
RNA sequencing of subchondral bone from patients that underwent a joint replacement surgery due to osteoarthritis.
Study
EGAS00001004476
-
Colorectal cancer cells possess an equipotent capacity to enter a developmental pausing-like state to survive chemotherapy
Study
EGAS00001004773
-
Complex patterns of genomic heterogeneity identified in 42 tumor samples and ctDNA of a pulmonary atypical carcinoid patient
Study
EGAS00001006530
-
Plasma ctDNA is a tumor tissue surrogate and enables clinical-genomic stratification of metastatic bladder cancer
Study
EGAS00001004615
-
Exome sequencing of EBV-driven lymphoma
Dataset
EGAD00001001347
-
Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG)
Study
phs002004
-
Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort second timepoint data
Study
EGAS50000001181
-
Memory-like HCV-specific CD8+ T cells retain a chronic scar after cure of chronic HCV infection
Study
EGAS00001004538