-
comprehensive genetic analysis and database construction for head and neck cancer
Study
JGAS000214
-
cfMeDIP data for 67 VPC samples
Dataset
EGAD00001008711
-
cfMeDIP data for 72 VPC samples for validation
Dataset
EGAD00001008737
-
PGDx elio™ plasma resolve assay: targeted sequencing analyses of plasma cfDNA
Dataset
EGAD00001009719
-
Oesophageal_Adenocarcinoma_Organoid_ATAC
Study
EGAS00001003890
-
Radiotherapy_induced_sarcoma
Study
EGAS00001000138
-
Genetic Factors associated with Conversion from Active Surveillance to Treatment for Prostate Cancer
Study
phs002056
-
ENOC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003266
-
Whole Genome Sequencing of Liver Cancers
Study
EGAS00001002408
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Study
EGAS00001000738
-
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
-
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Study
EGAS00001003493
-
Microbiota 16S sequencing study in NSCLC patients eligible for surgery without neoadjuvant treatment
Study
EGAS00001004728
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Phase Ib of olaparib and capivasertib
Study
EGAS00001004930
-
Multi-omics analysis of serial samples from metastatic TNBC patients on PARP inhibitor monotherapy provide insight into rational PARP inhibitor therapy combinations
Study
EGAS00001005479
-
Persistent Mutation Burden Drives Sustained Anti-Tumor Immune Responses
Study
EGAS00001006660
-
exploration of biomarkers discriminating squamous cell carcinoma from other lung cancers
Study
JGAS000488
-
Single-cell multi-omics of relapse/refractory multiple myeloma patients (Hipo K08K/H067/K43R)
Study
EGAS00001006538
-
SYNTHETIC DATA: EOSC4Cancer Colorectal Cancer (CRC) synthetic Whole Genome Sequencing dataset
Dataset
EGAD50000000384
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
NHLBI TOPMed - NHGRI CCDG: Malmo Preventive Project (MPP)
Study
phs001544
-
DNA Double Strand Breaks in KMT2A-Rearranged AML patients
Study
phs002804
-
Health Professionals Follow-Up Study
Study
phs002460
-
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
THAP11 mutations in a patient with a cblX-like phenotype implicates THAP11 in the regulation of cobalamin metabolism and early vertebrate development
Study
EGAS00001002201
-
Profiling the unique protective properties of intracranial arterial endothelial cells
Study
EGAS00001004479
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM67 WES
Study
EGAS00001004555
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma
Study
EGAS00001004564
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM066-WES
Study
EGAS00001004567
-
Molecular and clinical diversity in primary central nervous system lymphoma: a LOC Network study
Study
EGAS00001006191
-
DNA methylation-based prognostic subtypes of chordoma tumors in tissue
Study
EGAS00001006406
-
Multi-omic analysis of the tumor microenvironment shows clinical correlations in Ph1 study of atezolizumab +/- SoC in MM
Study
EGAS00001007286
-
Stromal-induced epithelial-mesenchymal transition induces drug resistance in acute lymphoblastic leukemia
Study
EGAS00001006120
-
Resistance to Checkpoint Blockade Therapy Through Inactivation of Antigen Presentation
Study
phs001427
-
Peripheral Blood Transcriptome Analysis of ALS Patients
Study
phs002055
-
Analysis of Donor Pancreata Defines the Transcriptomic Signature and Microenvironment of Early Neoplastic Pancreatic Lesions
Study
phs003229
-
TMD-AMKL targeted follow-up part 2
Dataset
EGAD00001000879
-
SOFT study - sequencing premenopausal breast cancer (2017-11-22)
Dataset
EGAD00001003811
-
Adenoma development in familial adenomatous polyposis and MUTYH‐associated polyposis: somatic landscape and driver genes
Dataset
EGAD00001004332
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Dataset
EGAD00001004501
-
MutWP5: CRUK Mutographs of Cancer: Breast: BRCA Carriers (Targeted) (2020-01-29)
Dataset
EGAD00001005920
-
MutWP5: CRUK Mutographs of Cancer: Breast: BRCA Carriers (Exome) (2020-01-29)
Dataset
EGAD00001005921
-
Circulating cell-free DNA analyses for Patient Monitoring in Small Cell Lung Cancer
Dataset
EGAD00001007070
-
252 human breast cancer samples in WGS and WES
Dataset
EGAD00001007563
-
Development and Validation of a Prognostic and Predictive 32-Gene Signature for Gastric Cancer
Dataset
EGAD00001008091
-
Hubrecht Organoid Technology Colon Cancer Study
Dataset
EGAD00001008445