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A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
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Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
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Genome-wide identification of distinct miRNA-mRNA target regulation pairs in Non-Hodgkin lymphomas: a report from the ICGC MMML-Seq consortium
Study
EGAS00001001394
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Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
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Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
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Exome-sequencing of human B cell lymphoma cell lines
Study
EGAS00001001463
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TERT rearrangements are frequent in neuroblastoma and identify aggressive tumors
Study
EGAS00001001479
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WGS of MAPKi acquired resistant samples from patients and PDX models
Study
EGAS00001006874
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Transcriptomic analysis of liver CD8+ T cells
Study
EGAS00001006885
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Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks
Study
EGAS00001002571
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Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Study
EGAS00001006916
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Reduced Representation Bisulfite Sequencing (RRBS) in various tissues to discover DNA methylation markers for the diagnosis of breast and ovarian cancer.
Study
EGAS00001002609
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Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
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Genomic and transcriptomic profiling of signalling networks in follicular lymphoma
Study
EGAS00001002175
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Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
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Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
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Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
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Container Study for ICGC Malignant Lymphoma Master Study (MMML)
Study
EGAS00001001600
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The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
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BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
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Cancer sequencing for somatic variant calling
Study
EGAS00001007101
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Chondrosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000277
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46 patients primary malignant glioma cohort in Chinese population
Study
EGAS00001005583
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Spatial Transcriptomics on prostate cancer heterogeneity
Study
EGAS00001003001
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Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Study
EGAS00001001784
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Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
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BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs
Study
EGAS00001002298
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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
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THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Study
EGAS00001004243
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Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
-
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
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
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Mutational landscape of renal cell carcinoma with venous tumor thrombus
Study
EGAS00001001950
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Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
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Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission
Study
EGAS00001001973
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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
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miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
-
Gene fusion and transcriptomic landscapes of sarcomas
Study
EGAS00001002189
-
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