-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
Study
EGAS00001004093
-
Single-cell profiling reveals mechanisms of response to anti-PD-L1 versus anti-PD-L1 combined with anti-CTLA4 in head and neck squamous cell carcinoma
Study
EGAS50000000037
-
Germ Cell and Associated Heme Malignancies Evolve from a Common Shared Precursor
Study
phs002231
-
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625
-
GATA2 Deficiency
Study
phs002311
-
Integrated Genomic Analysis of Periampullary Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000895
-
Tandem DNA Repeats Activate hTERT Gene Transcription
Study
phs002428
-
Pre-Existing Skin-Resident CD8 and γδ T Cell Circuits Mediate Immune Response in Merkel Cell Carcinoma and Predict Immunotherapy Efficacy
Study
phs003629
-
Myelodysplastic_syndrome_whole_genomes
Study
EGAS00001000291
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Study
EGAS00001002257
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
Myeloproliferative_Disease_Whole_Genomes
Study
EGAS00001000290
-
Molecular analysis of circulating tumour cells identifies distinct profiles in chemosensitive and chemorefractory patients with small cell lung cancer
Study
EGAS00001001951
-
Genome-wide search for higher order epistasis as modifiers of treatment effects on bone mineral density in childhood cancer survivors
Study
EGAS00001002645
-
WES data from 165 tumor/germline samples with muscle invasive bladder cancer.
Study
EGAS00001004507
-
St. Jude Children’s Research Hospital – Washington University Pediatric Cancer Genome Project Steering Committee
Dac
EGAC00001000044
-
Somatic mutations, clonal architecture and genomic evolution in multiple myeloma
Dataset
EGAD00001000339
-
A practical guide for mutational signature analysis in hematological malignancies
Dataset
EGAD00001005028
-
Dataset for soft_tissue_tumor-EXON
Dataset
EGAD00001008897
-
Comparison of single/pooled CTCs and bulk exome sequencing
Dataset
EGAD00001009052
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Dataset
EGAD50000000277
-
Other NS tumors
Dataset
EGAD50000000299
-
Establishment of an integrated database for clinical and genomic data in cancer
Study
JGAS000206
-
Melanoma PEACE Dataset
Dataset
EGAD00001010877
-
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Study
EGAS50000000021
-
Transcriptional_analysis_of_cells_from_lungs
Study
EGAS00001002649
-
NEOPREDICT-Lung: longitudinal whole exome sequencing of non-small cell lung cancers under immunotherapy
Dataset
EGAD00001015362
-
Sebaceous carcinoma tumor/normal exome sequencing and transcriptome sequencing. Transcriptome sequencing of
Dataset
EGAD00001004016
-
(Epi)genetic Risk Architectures of Opioid-Dependent Brain
Study
phs002724
-
The cellular immune and airway epithelial profile throughout childhood and in response to COVID-19 at multi-omic single cell level.
Dataset
EGAD00001007718
-
Lactobacillus rhamnosus GG ATCC (LGG) as an immune adjuvant for influenza vaccination in the elderly
Study
phs000981
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype.
Study
EGAS00001004135
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
Enrichment of oral-derived bacteria in inflamed colorectal tumors and distinct associations of Fusobacterium in the mesenchymal subtype
Study
EGAS00001006757
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Study
phs001480
-
North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES)
Study
phs000827
-
Drug screening of patient-derived organoids from colorectal peritoneal metastases
Study
phs002023
-
Transformation of Dysplasia in Barrett's Esophagus
Study
phs002706
-
Molecular analysis of post-colonoscopy CRC (PCCRC)
Study
EGAS00001004686
-
RNA sequencing of CCO- and CCO+ human hepatocytes
Study
EGAS00001006984
-
NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021)
Study
EGAS00001002759
-
Unraveling metastatic progression of breast cancer
Study
EGAS00001000760
-
WXS of 147 lung cancer patients treated with immunotherapy
Study
EGAS00001003781
-
NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
-
Tobacco exposure and somatic mutations in normal human bronchial epithelium
Dataset
EGAD00001005193
-
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