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Whole exome sequencing of endometriod ovarian cancer tumours
Dataset
EGAD00001006389
-
Single-cell gene expression data from CD8+ T cells from two Austrian COVID19 patients stimulated with wildtype and mutant SARS-Cov-2 peptides
Dataset
EGAD00001006995
-
Dataset for the Pearl study
Dataset
EGAD00001007979
-
POETIC clinical Trial Ki67 Bookend Breast Cancer Targeted Exome and RNAseq Project
Dataset
EGAD00001010919
-
Organoid Derivation Project: WGS (2023-06-22)
Dataset
EGAD00001011090
-
Genomic gain of EBV's LMP-1 in NKTCL
Study
EGAS50000000260
-
Pooled Genome-Wide Analysis of Kidney Cancer Risk (KIDRISK)
Study
phs001271
-
Targeted capture, whole genome sequencing, and RNAseq to identify rearrangements in B-cell lymphomas
Study
EGAS50000000328
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR
Study
EGAS00001002132
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
-
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
EPICC: Evolutionary Predictions in Colorectal Cancer WGS-3
Dataset
EGAD00001008642
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases
Study
EGAS00001007136
-
Whole Exome Sequencing of Chronic Lymphocytic Leukemia
Study
phs000435
-
MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features
Study
phs002005
-
A New Pipeline to Predict and Confirm Tumor Neoantigens Predicts Better Response to Checkpoint Blockade
Study
phs002269
-
Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma
Study
phs001041
-
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Study
phs000579
-
MAP Kinase-Mutant Hematologic Malignancies and Their Therapeutic Resistance
Study
phs001864
-
Molecular Characterization of Hemimegalencephaly
Study
phs002156
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Study
EGAS00001002597
-
Genomic analysis Nasopharyngeal cancer through whole exome sequencing and whole genomic sequencing.
Study
EGAS00001002788
-
WGS___Exploration_of__mutational_processes_in_human_cancer_cell_lines
Study
EGAS00001002680
-
HSC_population_dynamics___CB001_samples
Study
EGAS00001003397
-
HSC_population_dynamics___KX007_samples
Study
EGAS00001004193
-
HSC_population_dynamics_CBD_samples
Study
EGAS00001003091
-
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
Study
EGAS00001003040
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
Deep amplicon sequencing to infer malignant clonal populations for The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Dataset
EGAD00001003986
-
SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Dataset
EGAD00001004135
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET) - Intratumoural immune heterogeneity
Dataset
EGAD00001006570
-
Spatially confined sub-tumor microenvironments in pancreatic cancer
Dataset
EGAD00001008155
-
WGS of TNBC PDXs
Dataset
EGAD00001008535
-
Whole genome sequencing
Dataset
EGAD00001009746
-
Diet driven microbial ecology underpins associations between cancer immunotherapy outcomes and the gut microbiome
Study
EGAS00001006982
-
Single-cell atlas of penile cancer reveals TP53 mutations as driver for an aggressive phenotype, irrespective of HPV status, and provides clues for treatment personalization
Study
EGAS50000000217
-
Development, maturation and maintenance of human prostate inferred from somatic mutations
Dataset
EGAD00001006591
-
HSC_population_dynamics_KSP_samples
Study
EGAS00001002762
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
CM067 WES - Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma
Dataset
EGAD00001007573
-
Evolution of an adenomacarcinoma in response to selection by targeted kinase inhibitors
Study
EGAS00000000074
-
pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody
Study
EGAS00001004196
-
Clinical relevance of somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated NSCLC patients treated with osimertinib
Study
EGAS00001004539
-
Sequencing-based counting and size profiling of plasma Epstein-Barr virus DNA enhance population screening of nasopharyngeal carcinoma.
Study
EGAS00001002707
-
Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing
Study
EGAS00001000642
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
-
Robust methylation-based classification of brain tumours using nanopore sequencing
Study
EGAS00001006540