-
Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
-
The genomic landscape of cutaneous squamous cell carcinoma from immunosuppressed and immunocompetent patients reveals common drivers and a novel mutational signature associated with chronic azathioprine exposure
Study
EGAS00001002612
-
miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
-
Dynamics of neoantigen landscape during immunotherapy
Study
EGAS00001002704
-
Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Study
EGAS00001002953
-
Exome sequencing of synchronous colorectal cancers
Study
EGAS00001003474
-
Utility of ctDNA to support patient selection for early phase clinical trials: The TARGET Study
Study
EGAS00001003407
-
DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Study
EGAS00001003731
-
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas
Study
EGAS00001004461
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
-
Mutations in the RAS/MAPK pathway drive replication repair deficient hypermutated tumors and confer sensitivity to MEK inhibition
Study
EGAS00001005008
-
A Proteogenomic Analysis of Clear Cell Renal Cell Carcinoma in a Chinese Population
Study
EGAS00001006005
-
Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab
Study
EGAS00001006004
-
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Study
EGAS00001005982
-
WGS of MAPKi acquired resistant samples from patients and PDX models
Study
EGAS00001006874
-
Preferential infiltration of unique Vγ9Jγ2‐Vδ2 T cells into glioblastoma multiforme
Dataset
EGAD00001004862
-
Whole genome and Whole exome sequencing of patient-derived xenograft models of endometrial cancer
Dataset
EGAD00001008326
-
Comparison of sequencing assays for sensitive detection of circulating tumour DNA in stage IA-IV breast cancer
Dataset
EGAD00001008589
-
Origination of Ovarian Cancer is Dependent on Specific Aneuploidy Landscape
Study
EGAS00001007220
-
Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with Constitutional Mismatch Repair Deficiency
Study
EGAS00001007660
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000160
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000162
-
Oxidative DNA damage and ubiquitin proteasome system dysfunction underpins neurodegeneration in young adults with a DNA repair disorder
Study
EGAS50000000158
-
Molecular Profiling and Sequential Somatic Mutation Shift in Hypermutator Tumors Harboring POLE Mutations
Study
JGAS000130
-
Karyotype Evolution in Response to Chemoradiotherapy and Upon Recurrence of Esophageal Adenocarcinomas
Study
EGAS00001007711
-
Adult granulosa cell tumor WGS data cohort with corresponding reference germline WGS data
Study
EGAS00001004249
-
Immune trajectory of response and adverse effect in immunotherapy-treated hepatocellular carcinoma
Study
EGAS00001004843
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Study
EGAS00001006631
-
GeneScreen, a Population Based, Targeted Genomic Screening Study
Study
phs001817
-
A Genome-wide Association Study (GWAS) of Risk for Osteosarcoma
Study
phs000734
-
Metastatic Colorectal Adenocarcinoma Tumor Purity Assessment from Whole Exome Sequencing Data
Study
phs003059
-
Structure of the Mucosal and Stool Microbiome in Lynch Syndrome
Study
phs002343
-
Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001004407
-
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Study
EGAS00001002936
-
Longitudinal Single-Cell Profiling Reveals Molecular Heterogeneity and Tumor-Immune Evolution in Refractory Mantle Cell Lymphoma
Study
EGAS00001005019
-
Spatial transcriptomics analysis of triple negative breast cancers
Study
EGAS50000000475
-
ATAC-Seq of inflamed and non-inflamed biopsies
Study
EGAS00001007344
-
Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project
Study
phs001436
-
Treatment stratification and biomarker validation using patient-derived head and neck cancer organoids
Study
EGAS00001007076
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
-
MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Study
EGAS00001003991
-
Comprehensive genomic analysis of colorectal cancer with microsatellite instability
Study
JGAS000113
-
Frequent post-treatment monitoring of colorectal cancer using individualized ctDNA validated by multi-regional molecular profiling
Study
JGAS000243
-
Analysis of mutational and proteomic heterogeneity of gastric cancer to monitor post-treatment tumor burden using circulating tumor DNA
Study
JGAS000231
-
Molecular Evolution of Cancer
Study
phs001255
-
Cerebrospinal fluid cfDNA sequencing for classification of central nervous system glioma
Study
EGAS50000000060
-
Amplicon_based_sequencing_of_drug_resistant_lung_cancer_cell_lines
Study
EGAS00001001675
-
Cylindromas_sun_protected_and_exposed
Study
EGAS00001002521
-
Clonal architecture and genomic features of smoking versus non-smoking oncogene-driven East-Asian non-small cell lung cancer
Study
EGAS00001006942
-
Imaging metabolic heterogeneity in breast cancer using hyperpolarized 13C-MRI
Study
EGAS00001004118
-
Use of Deep Sequencing to Dectect Clonal Mutations In Sun Exposed Skin Epidermis PART2
Dataset
EGAD00001000825
-
Use of Deep Sequencing to Dectect Clonal Mutations In Sun Exposed Skin Epidermis
Dataset
EGAD00001001090
-
Whole genome sequencing informs treatment decision of end-stage metastatic cutaneous angiosarcoma in a patient with Xeroderma Pigmentosum
Dataset
EGAD00001004786
-
Spatial whole exome sequencing of metastatic melanoma
Dataset
EGAD00001005819
-
Single cell transcriptomes of of primary tumors and normal endometrial derived organoids treated with DBZ
Dataset
EGAD00001006280
-
Dataset for soft_tissue_tumor-WHOLE_GENOME
Dataset
EGAD00001008900
-
Whole-genome sequencing on hepatocellular carcinoma with nodule-in-nodule appearance reveals stepwise cancer evolution
Study
JGAS000190
-
CALGB/SWOG 80405: Genome-Wide Association Study of Patients with Advanced or Metastatic Colorectal Cancer Treated with First-Line Chemotherapy Combined with Cetuximab and/or Bevacizumab
Study
phs003428
-
Transcriptome human nasal epithelium
Dataset
EGAD00001002226
-
Activation of Wnt/β-catenin signalling by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary gland basal cell adenoma - RNA
Dataset
EGAD00001015366
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
Structure and Diversity of Urinary Cell-Free DNA Informative of Host-Pathogen Interactions in Human Urinary Tract Infection
Study
phs001564
-
A Genome-Wide Association Study of Heroin Dependence
Study
phs000277
-
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
-
Determining genome-wide binding of ETS2 by CUT&RUN in primary human macrophages
Dataset
EGAD00001011349
-
Pseudotime_ordering_of_cell_cycle_state
Study
EGAS00001003293
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
Genetic characterization patients affected by Cancer of Unknown Primary
Study
EGAS00001006621
-
NLG-LBC-05 ctDNA project sequencing data
Dataset
EGAD00001009337
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 3)
Dataset
EGAD00001009888
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 7a)
Dataset
EGAD00001010845
-
Whole Genome Sequencing of Liver Cancers
Dataset
EGAD00001003281
-
Molecular underpinnings of dedifferentiation and aggressiveness in chromophobe renal cell carcinoma
Study
EGAS50000000287
-
Machine Learning Guided Signal Enrichment for Plasma Tumor-burden Monitoring Dataset
Dataset
EGAD00001011352
-
Circulating Tumor DNA in Checkpoint Inhibitor treated Lung Cancer
Study
EGAS00001004847
-
Spiradenocarcinoma
Study
EGAS00001001799
-
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
-
Combined MEK and BCL-2/XL inhibition is effective in high-grade serous ovarian cancer patient-derived xenograft models and BIM levels are predictive of responsiveness
Study
EGAS00001003427
-
Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Study
EGAS00001005572
-
Functional Mapping of AKT Signaling and Biomarkers of Response From the FAIRLANE Trial of Neoadjuvant Ipatasertib Plus Paclitaxel for Triple-Negative Breast Cancer
Study
EGAS00001005892
-
The University of Hong Kong Gastric Cancer Organoids RHO Signaling Study
Study
EGAS00001006252
-
Genome and gene analysis of gastrointestinal cancer and elucidation of its clinicopathological significance
Study
JGAS000233
-
Histone chaperone CHAF1A promotes proliferation and tumorigenicity in gastric cancer and impacts prognosis via context-depedent regulation of gene expression
Study
EGAS00001003064
-
National Cancer Institute (NCI) Non-Hodgkin Lymphoma Genome-wide Association Study (GWAS)
Study
phs000801
-
The ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge
Study
EGAS00001002092
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
Somatic_mutation_profiling_of_intestinal_crypts_from_IBD
Study
EGAS00001002896
-
Molecular origins of mpMRI visibility
Study
EGAS00001003179
-
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Study
EGAS00001000276
-
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
Study
EGAS00001004373
-
Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma
Study
EGAS00001005023
-
early-stage ESCC sequencing study
Study
EGAS00001006126
-
Clonal hematopoiesis is associated with adverse outcomes in patients with COVID-19
Study
EGAS00001006218
-
Whole-genome sequencing of gastric cancer 81 samples in the Japanese population.
Dataset
EGAD00001008610
-
cell-free DNA Whole Genome Sequencing of 3784 samples on MGI and Illumina platform
Dataset
EGAD00001009335
-
Genomic Data of Pediatric MDS
Dataset
EGAD00001007856
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Study
EGAS50000000191
-
WGS of T-cell and NK-cell lymphoma for ICGC (NKTL-SG)
Study
EGAS00001002398