-
An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients.
Study
EGAS00001000669
-
Oncogenic chimeric transcription factors drive tumor-specific transcription, processing, and translation of silent genomic regions
Study
EGAS00001006293
-
Effects of busulfan, fludarabine and clofarabine treatment on human small intestinal organoids generated from healthy donors
Study
EGAS00001007550
-
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Study
EGAS00001001795
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
Genomic Heterogeneity and the Small Renal Mass
Study
EGAS00001002919
-
Whole exome sequencing reveals the mutational spectrum of testicular germ cell tumours
Study
EGAS00001001084
-
Transcriptional_Consequences_of_Copy_Number_Changes_MY_HDBR_200531
Study
EGAS00001005100
-
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
-
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Study
EGAS00001004380
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Novel mutations in TOP2A in gliomas
Study
EGAS00001004556
-
single-stranded DNA study
Study
EGAS00001005093
-
Establishment and characterization of an Epstein-Barr virus-positive cell line from a non-keratinizing differentiated primary nasopharyngeal carcinoma
Study
EGAS00001007172
-
Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer
Study
phs001261
-
Immunoreactive_p53_areas_in_human_skin_2
Study
EGAS00001004463
-
Clonal Evolution of PPM1D Mutations in the Spectrum of Myeloid Disorders
Study
EGAS50000000840
-
PD1-targeted delivery of an IL-2 variant induces a multifaceted anti-tumoral T cell response in human lung cancer
Study
EGAS50000000396
-
Chordoma_Targeted_Sequencing_Study
Study
EGAS00001000280
-
Osteosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000278
-
Meningioma_Targeted_Sequencing_Study
Study
EGAS00001000282
-
Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer
Study
EGAS00001005981
-
Molecular heterogeneity and commonalities in pancreatic cancer precursors with gastric and intestinal phenotype
Study
EGAS00001006793
-
Bone marrow single cell genomics from blood cancer samples
Study
EGAS00001007332
-
Clinical Sequencing Exploratory Research (CSER): Clinical sequencing in cancer: Clinical, ethical, and technological studies
Study
phs000999
-
Single Cell RNA-Seq Reveals Malignant and Stromal Programs Associated with Metastasis in Head and Neck Cancer
Study
phs001474
-
Collagen XVII Promotes Pancreatic Cancer Through Regulation of PIK3R5
Study
phs003641
-
Ultra-sensitive tumor-informed ctDNA monitoring of treatment response in advanced esophagogastric cancer patients
Study
EGAS50000001224
-
Plasma-Seq of patients with metastatic prostate cancer
Study
EGAS00001000451
-
Non-muscle Invasive Bladder Cancer Molecular Subtypes Predict Differential Response to Intravesical Bacillus Calmette-Guérin
Study
EGAS00001006879
-
ProHealth: Kaiser Permanente Genome-wide Association Study of Prostate Cancer
Study
phs001221
-
Exceptional Responders Initiative
Study
phs001145
-
Identification of Somatic Changes in Tumors from Fanconi Anemia Patients
Study
phs002652
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
Neoadjuvant atezolizumab plus chemotherapy in gastric and gastroesophageal junction adenocarcinoma: the phase 2 PANDA trial
Study
EGAS50000000168
-
Automated machine-learning approach for next generation profiling of sequence alterations, mutation burden, microsatellite instability, and structural variants in human cancers
Study
EGAS00001005556
-
TK-EPN862 - Patient-dervied xenograft model of Posterior Fossa A Ependymoma - RNAseq
Study
EGAS00001006844
-
Multi-Modal Single-Cell, Spatial, and Genomic Analyses of Human Non-Small Cell Lung Cancer Brain Metastases
Study
phs003865
-
INTEGRATIVE MOLECULAR ANALYSIS OF SKIN TUMORS FROM CYLD CUTANEOUS SYNDROME PATIENTS
Study
EGAS50000000247
-
Childhood Cancer Data Initiative (CCDI): Clonal Evolution During Metastatic Spread in High-Risk Neuroblastoma
Study
phs003111
-
National Cancer Institute (NCI) Waldenstrom Macroglobulinemia Genome-wide Association Study
Study
phs001284
-
Subclonal variation in patients with pediatric T-lymphoblastic leukemia (T-ALL)
Study
EGAS50000000794
-
Clonal hematopoiesis in rheumatoid arthritis
Study
EGAS50000000890
-
Melanoma_multi_site_metastases
Study
EGAS00001001348
-
Somatic Inactivation of Breast Cancer Predisposition Genes in Tumours Associated with Pathogenic Germline Variants
Study
EGAS00001006532
-
WGS___Mutant_clone_mapping_in_normal_oesohagus_and_skin
Study
EGAS00001002416
-
Multiple_Myeloma_Diagnosis_to_Relapse_study_samples
Study
EGAS00001001299
-
Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals.
Study
EGAS00001002933
-
Lymphoctye_colony_WGS
Study
EGAS00001002948
-
FAM50A_Disruption_in_TOV21G_Cells___RNAseq
Study
EGAS00001004156
-
Single_cell_resolution_of_human_CNV_body_map
Study
EGAS00001003162
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
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
-
Karyotype Evolution in Response to Chemoradiotherapy and Upon Recurrence of Esophageal Adenocarcinomas
Study
EGAS00001007711
-
Next generation sequencing of diffuse intrinsic pontine glioma samples to identify recurrent mutations, variations, and expression patterns to define novel therapies
Study
phs001526
-
GeneScreen, a Population Based, Targeted Genomic Screening Study
Study
phs001817
-
Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia
Study
phs001372
-
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
-
Integrative Age-Related Changes in Genome and Epigenome in Human Lung in Relation to Smoking
Study
phs003317
-
Genomic Profiling of Melanoma
Study
phs000933
-
Structure of the Mucosal and Stool Microbiome in Lynch Syndrome
Study
phs002343
-
Ipilimumab and Decitabine in Treating Patients With Relapsed or Refractory Myelodysplastic Syndrome or Acute Myeloid Leukemia
Study
phs003015
-
MP2PRT: Genomic and Molecular Characterization of Biomarkers Associated with Tumor Angiogenesis, DNA Repair, and Immunologic Tolerance using Samples from the NRG Oncology Phase 3 Randomized Trial, GOG-0240 (NCT00803062)
Study
phs002293
-
California Teachers Study (CTS): Whole Genome Sequences From Under-Represented Populations
Study
phs002918
-
MP2PRT-MNG: Identifying Novel Molecular Markers of Response to Radiotherapy in Meningiomas Using Samples from the RTOG-0539 (NCT00895622)
Study
phs003707
-
Nivolumab plus chemotherapy or ipilimumab in gastroesophageal cancer: CheckMate 649 biomarker analyses
Study
EGAS50000000747
-
Spatial Transcriptomics Uncovers Tumor Microenvironment-Based Subtypes in Invasive Lobular Carcinoma
Study
EGAS50000001001
-
Identifying genetic variants that alter TCR usage in the peripheral repertoire
Study
EGAS00001008189
-
Molecular Profiling and Sequential Somatic Mutation Shift in Hypermutator Tumors Harboring POLE Mutations
Study
JGAS000130
-
Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
-
Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
Study
EGAS00001003822
-
Adult granulosa cell tumor WGS data cohort with corresponding reference germline WGS data
Study
EGAS00001004249
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
-
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
-
Systematic kinase inhibitor profiling identifies CDK9 as a synthetic lethal target in NUT midline carcinoma
Study
EGAS00001002588
-
Dynamics of neoantigen landscape during immunotherapy
Study
EGAS00001002704
-
CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
Single-cell RNA-seq of immune cells sorted from human melanoma tumors
Study
EGAS00001003363
-
Utility of ctDNA to support patient selection for early phase clinical trials: The TARGET Study
Study
EGAS00001003407
-
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
-
Exome and RNA sequencing data from 32 ocular and extraocular sebaceous carcinomas
Study
EGAS00001002869
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552
-
Immune trajectory of response and adverse effect in immunotherapy-treated hepatocellular carcinoma
Study
EGAS00001004843
-
Longitudinal Single-Cell Profiling Reveals Molecular Heterogeneity and Tumor-Immune Evolution in Refractory Mantle Cell Lymphoma
Study
EGAS00001005019
-
Recurrent adeno-associated virus 2-related insertional mutagenesis in human hepatocellular carcinomas
Study
EGAS00001001284
-
Engineering large chromosomal deletions by CRISPR-Cas9
Study
EGAS00001005134
-
DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Study
EGAS00001003731
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325
-
Rare occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers
Study
EGAS00001005909
-
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Study
EGAS00001002936
-
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas
Study
EGAS00001004461
-
Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Study
EGAS00001002953
-
Mutations in the RAS/MAPK pathway drive replication repair deficient hypermutated tumors and confer sensitivity to MEK inhibition
Study
EGAS00001005008
-
CRISPR transduction of iPS cells
Study
EGAS00001005102