-
WES_SCLC_MDACC
Dataset
EGAD00001007004
-
Whole exome data from PMID27216186
Dataset
EGAD00001008149
-
Triple negative breast cancer matched patient and pdx dataset
Dataset
EGAD00001009046
-
Genome-wide 5-mC profiling in plasma of metastatic ALK-rearranged non-small cell lung cancer (NSCLC) patients receiving tyrosine kinase inhibitor therapy.
Dataset
EGAD00001009412
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 7b)
Dataset
EGAD00001011086
-
The effects of bioinformatics preprocessing on cell-free DNA analysis
Dataset
EGAD50000000213
-
Development of actionable molecular targets and/or biomarkers for prognostication and patient stratification in gynecological cancer based on whole-exome sequencing and epigenomic analysis
Study
JGAS000174
-
Warm_Autopsy_Single_Cell_X10
Study
EGAS00001001698
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Axiom GWAS
Study
phs001856
-
cfRRBS methylation profiling of cfDNA from cerebrospinal fluid from pediatric CNS tumor patients
Dataset
EGAD50000000554
-
To profile the landscape of sebaceous tumours_WES
Dataset
EGAD00001015367
-
Neoantigen Immunogenicity Landscapes and Evolution of Tumor Ecosystems During Immunotherapy with Nivolumab
Dataset
EGAD00001011302
-
PGDx elio™ plasma resolve assay: targeted sequencing analyses of WBC DNA
Dataset
EGAD00001009721
-
Yemen_and_Chad_Genotyping
Study
EGAS00001001231
-
Whole Genome Sequencing of Multiple Myeloma patients treated with T-cell redirecting immunotherapies
Dataset
EGAD50000000776
-
BLUEPRINT EpiVar ChIP-seq in lineage specifying transcription factors
Dataset
EGAD00001004571
-
1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors.
Study
EGAS00001003250
-
Evolutionary dynamics of residual disease in human glioblastoma
Study
EGAS00001003043
-
National Cancer Institute Clinical and Laboratory Analysis of Familial Cancer
Study
phs001935
-
Targeting PTPRK-RSPO3 colon tumours promotesdifferentiation and loss of stem-cell function
Study
EGAS00001001462
-
WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
-
Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability
Study
EGAS00001000599
-
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
-
A PROSTATE TUMORGRAFT PANEL TO ACCELERATE PRECISION MEDICINE
Study
EGAS00001007033
-
CCOC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003265
-
WES dataset of 20 pre-post paired neoadjuvant chemotherapy treated breast cancer samples
Dataset
EGAD00001008442
-
Southern African Prostate Cancer Study (SAPCS) Ethnic Disparity
Dataset
EGAD00001009067
-
Whole-Exome Sequencing and Targeted DNA Sequencing of Matched Ocular Melanocytosis and Uveal Melanoma
Study
phs001835
-
Identification of Recurrent NAB2-STAT6 Gene Fusions in Solitary Fibrous Tumor by Integrative Sequencing
Study
phs000567
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Study
EGAS00001003517
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___single_cell_RNA_sequencing
Study
EGAS00001003519
-
Cergentis FFPE-TLC
Study
EGAS50000000427
-
Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis
Study
EGAS50000000591
-
BPH Tissues for Cell Culture and Analysis - A Patient-Derived Xenograft Model Using Benign Prostatic Tissues
Study
phs003692
-
NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Study
phs001515
-
Massively parallel nanowell-based single-cell gene expression profiling
Study
EGAS00001002320
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Study
EGAS00001003950
-
Whole Tumor spatial heterogeneity in metastatic melanoma
Study
EGAS00001003292
-
Characterizing the Role of the Immune Microenvironment in Multiple Myeloma Progression at a Single Cell Level
Study
phs002756
-
MILK-Omics: Systems Biology of Human Milk and Its Links to Maternal and Infant Health
Study
phs003408
-
Mutational landscape and patterns of clonal evolution in relapsed pediatric acute lymphoblastic leukemia
Study
EGAS00001003975
-
Kids First and INCLUDE: Down Syndrome, Heart Defects, and Acute Lymphoblastic Leukemia
Study
phs002330
-
Analyzing Somatic Mutagenesis in Systemic Sclerosis
Study
phs003700
-
Clinical outcomes and immune correlates of response to nivolumab plus chemoradiotherapy in women with locally-advanced cervical cancer – NiCOL study
Study
EGAS00001007297
-
Mutational landscape of normal epithelial cells in Lynch Syndrome patients
Dataset
EGAD00001008092
-
Efficacy of two different FGFR-inhibitors in a patient with extrahepatic cholangiocarcinoma harboring an FGFR2 mutation
Study
EGAS50000000015
-
Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation
Study
EGAS00001004013
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067