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Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Study
EGAS00001002874
-
Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Study
EGAS00001002908
-
Genomic Heterogeneity and the Small Renal Mass
Study
EGAS00001002919
-
SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Study
EGAS00001002920
-
Somatic point mutation data from microsatellite unstable colorectal cancers
Study
EGAS00001003101
-
The spatio-temporal evolution of lymph node spread in early breast cancer
Study
EGAS00001002947
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Study
EGAS00001002953
-
Whole-genome sequencing reveals genomic signatures associated with the inflammatory microenvironments in Chinese NSCLC patients
Study
EGAS00001002954
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
Targeted sequencing about core genes involved in telomere biology in colorectal cancer patients
Study
EGAS00001002977
-
Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
-
Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines
Study
EGAS00001002998
-
Biallelic tumor suppressor loss and DNA repair defects in de novo small cell prostate cancer
Study
EGAS00001003007
-
Age-related remodeling of apparently normal esophageal epithelia by common cancer drivers
Study
EGAS00001003008
-
CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___WGS
Study
EGAS00001003012
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___BD___WGS
Study
EGAS00001003014
-
Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers
Study
EGAS00001003119
-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Identification of recurrent mutations in Cushing’s disease
Study
EGAS00001003029
-
AUBTRG - Whole Exome Sequencing of Diffuse Glioma Samples
Study
EGAS00001003035
-
Recurrent loss of heterozygosity correlates with clinical outcome in pancreatic neuroendocrine cancer
Study
EGAS00001003038
-
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
Study
EGAS00001003040
-
Evolutionary dynamics of residual disease in human glioblastoma
Study
EGAS00001003043
-
Whole exome DNA sequence profiling of spatial biopsies of high grade serous epithelial ovarian cancer
Study
EGAS00001003048
-
Ewings Sarcoma RNA-Seq
Study
EGAS00001003062
-
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high risk disease
Study
EGAS00001003071
-
Parallel Detections of Somatic Gene Mutations in Surgically Resected Tumor tissues and Matched Plasma Specimens in Early-Stages of Primary Breast Cancer
Study
EGAS00001003075
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___TPS___WGS
Study
EGAS00001003089
-
HSC_population_dynamics_CBD_samples
Study
EGAS00001003091
-
Somatic mutations in endometriosis and normal uterine endometrium
Study
EGAS00001003095
-
Circulating cell-free DNA analysis in Small Cell Lung Cancer
Study
EGAS00001003110
-
Organoid Models of Human Liver Cancers Derived from Tumor Needle Biopsies
Study
EGAS00001003115
-
BS-seq in plasma of CRC patients
Study
EGAS00001003117
-
Whole exome sequencing of small cell neuroendocrine cancer of the cervix
Study
EGAS00001003142
-
DNA Methylation-based diagnostic biomarkers for ESCC in Han Chinese population
Study
EGAS00001003158
-
Tumor-associated preferred end coordinates and somatic variants as signatures of circulating tumor DNA
Study
EGAS00001003160
-
Primary breast tumor heterogeneity through therapy
Study
EGAS00001003168
-
“Castration-persistence” is a distinct state of tolerance to androgen receptor targeting therapies in prostate cancer
Study
EGAS00001003172
-
Primary breast cancers and paired brain metastases sequencing study
Study
EGAS00001003173
-
Study the differences at the trascriptome level between iNKT and T cells
Study
EGAS00001003176
-
Genome-wide association study of cervical cancer in East Asian populations
Study
EGAS00001003199
-
Exploiting evolutionary steering in cancer therapy
Study
EGAS00001003200
-
RNA-sequencing of Non-muscle Invasive Bladder cancer (NMIBC)
Study
EGAS00001004358
-
Oncogenic fate conversion by PRDM16s causes acute myeloid leukemia
Study
EGAS00001003235
-
Fibroblast heterogeneity drives metastatic spread in breast cancer through distinct mechanisms
Study
EGAS00001003238
-
1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors.
Study
EGAS00001003250
-
A Study to Evaluate Denosumab in Young Patients With Primary Breast Cancer (D-Beyond)
Study
EGAS00001003252
-
Molecular profiling of longitudinally observed small colorectal polyps: a cohort study
Study
EGAS00001003284
-
Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness
Study
EGAS00001003288
-
Whole genome sequencing of tumour and matched normal from patients with family history of breast cancer
Study
EGAS00001003305
-
STM4 - Mouliere et al, 2018. Enhanced detection of circulating tumor DNA by fragment size analysis
Study
EGAS00001004418
-
Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer
Study
EGAS00001003306
-
Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer RNA-Seq
Study
EGAS00001003307
-
SNP array datas of 'Matched' cancer/PNE
Study
EGAS00001003331
-
Exome sequencing of a novel cervical cancer cell line
Study
EGAS00001003343
-
CAF-S3 subset in human breast and ovarian cancers
Study
EGAS00001003344
-
Evaluation of commercial Guardant360 ctDNA test in metastatic prostate cancer
Study
EGAS00001003352
-
Non-coding RNAs in breast cancer
Study
EGAS00001003353
-
Personalised Mapping of Tumour Development in Synchronous Colorectal Cancer Patients
Study
EGAS00001004413
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Study
EGAS00001003367
-
organoid data of colorectal cancers
Study
EGAS00001003360
-
Single-cell RNA-seq of immune cells sorted from human melanoma tumors
Study
EGAS00001003363
-
DAC for integrated genomics of metastatic prostate cancer
Dac
EGAC00001000230
-
Extreme intratumor heterogeneity and driver evolution in mismatch repair deficient gastro-esophageal cancer
Study
EGAS00001003434
-
Detection of mutational patterns in cell free DNA (cfDNA) of colorectal cancer by custom amplicon sequencing
Study
EGAS00001003382
-
Utility of ctDNA to support patient selection for early phase clinical trials: The TARGET Study
Study
EGAS00001003407
-
Whole genome sequencing of Ewings Sarcoma
Study
EGAS00001003385
-
Sequencing Study in COPD cases and controls
Study
EGAS00001003406