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The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Study
EGAS00001001964
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Identification of recurrent mutations in Cushing’s disease
Study
EGAS00001003029
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IMCISION DNAseq
Study
EGAS00001005466
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Whole genome and whole transcriptome sequencing of Hepatosplenic T Cell Lymphoma tumor.
Study
EGAS00001003775
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Integrated genomic analyses reveal molecular correlates of clinical response and resistance to atezolizumab in combination with bevacizumab in advanced hepatocellular carcinoma
Study
EGAS00001005503
-
Immune profiling reveals enrichment of distinct immune signatures in high-risk oral potentially malignant disorders
Study
EGAS00001005520
-
Neuroblastoma sequencing data
Study
EGAS00001005602
-
Melanoma_brain_metastases
Study
EGAS00001002107
-
Single-cell RNA-seq data of the tumor microenvironment of lymphocyte-rich Hodgkin lymphoma and other Hodgkin lymphoma subtypes
Study
EGAS00001005541
-
RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics
Study
EGAS00001005581
-
RNA sequencing CYLD cutaneous syndrome
Study
EGAS00001003841
-
46 patients primary malignant glioma cohort in Chinese population
Study
EGAS00001005583
-
A single-cell atlas of human glioma
Study
EGAS00001003845
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Whole-transcriptome sequencing of hepatocellular carcinoma biopsies (TACE study)
Study
EGAS00001005558
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A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus.
Study
EGAS00001002334
-
Whole genome and exome sequencing data of invasive micropapillary carcinoma of breast
Study
EGAS00001005902
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UK renal cancer samples genotyped on Illumina OmniExpress BeadChip
Study
EGAS00001002336
-
Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Study
EGAS00001003860
-
Pre-neoplastic somatic mutations including MYD88L265P in lymphoplasmacytic lymphoma
Study
EGAS00001005656
-
WGS of T-cell and NK-cell lymphoma for ICGC (NKTL-SG)
Study
EGAS00001002398
-
Epigenome wide DNA methylation assay of gingivo-buccal oral squamous cell carcinoma using single base resolution high throughput array
Study
EGAS00001003896
-
Exome sequencing of pseudomyxoma peritonei
Study
EGAS00001002418
-
The genomic landscape of germinal center derived B-cell lymphomas other than follicular, diffuse-large B-cell and Burkitt lymphom
Study
EGAS00001002422
-
Cell fate mapping of human glioblastoma reveals an invariant stem cell hierarchy pre- and post-treatment
Study
EGAS00001002424
-
MM samples for epigenomic translocation of H3K4me3 broad domains following super-enhancer hijacking
Study
EGAS00001005684
-
HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
-
A combined circulating tumor DNA and protein biomarker-based liquid biopsy for the earlier detection of pancreatic cancer
Study
EGAS00001002444
-
Mutational signatures of aflatoxin
Study
EGAS00001002490
-
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Study
EGAS00001002495
-
Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Study
EGAS00001002504
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Study
EGAS00001002517
-
Brain_Disease_Wellcome_Leap_Delta_Tissue_Spatial
Study
EGAS00001005801
-
Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
-
SCC tumor sequencing
Study
EGAS00001003988
-
MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Study
EGAS00001003991
-
Whole-genome bisulfite sequencing analysis of low-grade astrocytomas in the ICGC PedBrain Tumor Project
Study
EGAS00001004019
-
Comparative genomics research for Chinese colorectal cancer
Study
EGAS00001002607
-
Somatic_mutation_and_clonal_evolution_in_the_human_pancreas___WGS
Study
EGAS00001002626
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017)
Study
EGAS00001002670
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
-
Alternative splicing isoforms in patient-derived hepatocellular carcinoma cells
Study
EGAS00001002697
-
Extensive three-dimensional intratumor proteomic heterogeneity revealed by multiregion sampling in high-grade serous ovarian tumor specimens
Study
EGAS00001005786
-
Brain_Disease_Wellcome_Leap_Delta_Tissue_DNA
Study
EGAS00001005799
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
Single-cell RNA sequencing of 22 Hodgkin lymphoma tumors and 5 reactive lymph nodes
Study
EGAS00001004085
-
Exon4-mutations in KRAS Affect MEK-ERK and Pi3K-AKT Signaling in Multiple Myeloma
Study
EGAS00001004110
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836