-
WES cutaneous and uveal melanoma liver metastases
Study
EGAS00001004795
-
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
Whole genome sequencing of metastatic melanomas from a patient with primary resistance to BRAF inhibition
Study
EGAS00001000580
-
Neuroblastoma Cell Line Circle-seq
Study
EGAS00001004796
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Study
EGAS00001000643
-
Institut Curie Neuroblastoma data access Committee
Dac
EGAC00001000319
-
CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
-
FACS sorting of ploidy populations in an undifferentiated soft tissue sarcoma for RRBS
Study
EGAS00001006143
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
Validation of a targeted sequencing panel for multiple myeloma
Study
EGAS00001006164
-
Small molecule inhibitors of LOXL synergize with 5-AZA to restore erythropoiesis in myeloid neoplasms
Study
EGAS00001006174
-
Study of pediatric hepatocellular carcinoma caused by bile salt export pump deficiency
Study
EGAS00001000749
-
Primary Neuroblastoma Circle-seq
Study
EGAS00001004797
-
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Study
EGAS00001000750
-
Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
-
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884
-
Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
-
Genomic analysis of seminomas
Study
EGAS00001000943
-
An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup
Study
EGAS00001001000
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
Targeted Gene Panel for 171 PTCLs
Study
EGAS00001002740
-
The Berlin (BLN) panel of glioblastoma cell lines: RNAseq of human gliomasphere cell lines and matched parental tumors
Study
EGAS00001001167
-
Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
-
Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
-
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma
Study
EGAS00001001190
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
-
MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Study
EGAS00001001199
-
Anaplastic oligodendroglioma exome and RNA sequencing data
Study
EGAS00001001209
-
Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Study
EGAS00001001244
-
Tracking the genomic evolution of esophageal adenocarcinoma through neoadjuvant chemotherapy
Study
EGAS00001001254
-
Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
-
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
-
Whole exome sequencing of papillary thyroid carcinoma in the Chinese population
Study
EGAS00001001268
-
MD Anderson Melanoma Genomic Medicine
Dac
EGAC00001000324
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001001293
-
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
-
Genomic analysis of HPV positive versus HPV negative esophageal adenocarcinoma
Study
EGAS00001001340
-
Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Study
EGAS00001001353
-
A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
-
Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
-
Genome-wide identification of distinct miRNA-mRNA target regulation pairs in Non-Hodgkin lymphomas: a report from the ICGC MMML-Seq consortium
Study
EGAS00001001394
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
Exome-sequencing of human B cell lymphoma cell lines
Study
EGAS00001001463
-
TERT rearrangements are frequent in neuroblastoma and identify aggressive tumors
Study
EGAS00001001479
-
WGS of MAPKi acquired resistant samples from patients and PDX models
Study
EGAS00001006874
-
Transcriptomic analysis of liver CD8+ T cells
Study
EGAS00001006885
-
Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks
Study
EGAS00001002571
-
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Study
EGAS00001006916
-
Reduced Representation Bisulfite Sequencing (RRBS) in various tissues to discover DNA methylation markers for the diagnosis of breast and ovarian cancer.
Study
EGAS00001002609
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Genomic and transcriptomic profiling of signalling networks in follicular lymphoma
Study
EGAS00001002175
-
Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
-
Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Container Study for ICGC Malignant Lymphoma Master Study (MMML)
Study
EGAS00001001600
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
Cancer sequencing for somatic variant calling
Study
EGAS00001007101
-
Chondrosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000277
-
46 patients primary malignant glioma cohort in Chinese population
Study
EGAS00001005583
-
Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Study
EGAS00001001784
-
Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
-
BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs
Study
EGAS00001002298
-
Mesothelioma Genomics Study - WGS tumour/normal pairs
Study
EGAS00001002299
-
UK renal cancer samples genotyped on Illumina OmniExpress BeadChip
Study
EGAS00001002336
-
glioblastoma single cell RNAseq
Study
EGAS00001006236
-
THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Study
EGAS00001004243
-
Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
-
Spatial and Temporal Homogeneity of Driver Mutations in Diffuse Intrinsic Pointine Glioma
Study
EGAS00001001654
-
33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Study
EGAS00001001658
-
Mutational landscape of renal cell carcinoma with venous tumor thrombus
Study
EGAS00001001950
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission
Study
EGAS00001001973
-
Prognostic relevance of microenvironmental factors CD163 and CD8 combined with EZH2 and chromosome 18 gain in a validation cohort of follicular lymphoma patients of the Lunenburg Lymphoma Biomarker Consortium
Study
EGAS00001002049
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
-
miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
-
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Study
EGAS00001002192
-
HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
-
Sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001002314
-
Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Study
EGAS00001002326
-
A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus.
Study
EGAS00001002334
-
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Study
EGAS00001002337
-
whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
-
Exome sequencing of pseudomyxoma peritonei
Study
EGAS00001002418
-
Whole genome sequencing identified biomarker of response to PD1 blockade in Natural-killer/T-cell lymphoma
Study
EGAS00001002420
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
Deep single-cell RNA sequencing data for 12346 T cells from tumour, adjacent normal tissue and peripheral blood of treatment-naive NSCLC patients
Study
EGAS00001002430
-
The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Study
EGAS00001002432
-
Genomic landscape of Chordoid Glioma
Study
EGAS00001002433
-
Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma
Study
EGAS00001002443
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
Cell motility and migration as determinants of stem cell efficacy
Study
EGAS00001002478
-
Mutational signatures of aflatoxin
Study
EGAS00001002490
-
Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Study
EGAS00001002495
-
Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma.
Study
EGAS00001002501
-
Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Study
EGAS00001002504
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538