-
Whole_Exome_PC9_and_A375
Study
EGAS00001002493
-
The_genomic_architecture_of_mesothelioma_
Study
EGAS00001000353
-
Diverse modes of genomic alterations in hepatocellular carcinoma
Study
EGAS00001000824
-
Chordoma_Sequencing_Project_Whole_Genome
Study
EGAS00001000409
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
Feasibility Study to Identify the Optimal Adjuvant Combination Scheme of Ipilimumab and Nivolumab (OpACIN) in resectable stage III melanoma patients
Study
EGAS00001003099
-
ChIP_sequencing_in_Cancer_Cell_Lines
Study
EGAS00001000203
-
ICGC Oesophageal adenocarcinoma - pilot samples
Study
EGAS00001000559
-
Tumor-associated preferred end coordinates and somatic variants as signatures of circulating tumor DNA
Study
EGAS00001003160
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
-
The molecular landscape of glioma in patients with Neurofibromatosis 1.
Study
EGAS00001003186
-
Integrative genomic profiling of hepatocellular adenomas reveals recurrent FRK activating mutations and mutational processes of malignant transformation
Study
EGAS00001000679
-
UQCCR/QCMG brain metastasis sequence analysis
Study
EGAS00001000722
-
Osteosarcoma_X10
Study
EGAS00001002167
-
ICGC Oesophageal adenocarcinoma - lymph-node samples
Study
EGAS00001000727
-
Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
-
Comprehensive miRNA Sequence Analysis Reveals Survival Differences in Diffuse Large B-cell Lymphoma Patients
Study
EGAS00001001025
-
Cross-species genomics identifies TAF12, NFYC and RAD54L as novel choroid plexus carcinoma oncogenes
Study
EGAS00001000961
-
463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA.
Study
EGAS00001001147
-
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982
-
An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup
Study
EGAS00001001000
-
Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
-
MGA-NUTM1 fusion in high grade spindle cell sarcoma
Study
EGAS00001003341
-
Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
-
Uveal melanoma patient with germline MBD4 nonsense mutation
Study
EGAS00001003362
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
Deciphering the mutational landscape and the genome organization of LMS
Study
EGAS00001001262
-
Whole exome sequencing of papillary thyroid carcinoma in the Chinese population
Study
EGAS00001001268
-
Genomic and transcriptomic profiling of signalling networks in follicular lymphoma
Study
EGAS00001002175
-
Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Study
EGAS00001001487
-
BAP1_sequence_of_uveal_melanoma_cell_lines
Study
EGAS00001001520
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Ewings_Sarcoma_RNA_seq_drug_sensitivity
Study
EGAS00001000419
-
Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma.
Study
EGAS00001002501
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Study
EGAS00001003481
-
Radiotherapy_induced_Sarcoma_exome
Study
EGAS00001000194
-
Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
-
Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
-
Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
-
UAMS Smoldering Myeloma Timeline Cohort
Study
EGAS00001003687
-
Human_primary_melanoma_project
Study
EGAS00001002409
-
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
-
Angiosarcoma_whole_exome
Study
EGAS00001000588
-
Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Study
EGAS00001001878
-
PLCG1 R707Q mutation is counter selected under targeted therapy in a patient with a hepatic angiosarcoma
Study
EGAS00001001281
-
EATL-II STUDY
Study
EGAS00001001879
-
Spatiotemporal genomic architecture informs precision oncology in glioblsatoma
Study
EGAS00001001880
-
Genetic landscape of relapsed DLBCL
Study
EGAS00001001553
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Methylation CYLD cutaneous syndrome
Study
EGAS00001003800
-
Genomic Analysis of Primary Plasma Cell Leukemia reveals Complex Structural Alterations and High Risk Mutational Patterns
Study
EGAS00001003834
-
Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform
Study
EGAS00001003846
-
Automated system for scoring hematoxylin and eosin-stained ovarian cancer sections by identifying single cells uncovered that stromal cell ratio is a significant predictor for overall survival and progression-free survival.
Study
EGAS00001001694
-
Modeling glioblastoma invasion using human brain organoids and single-cell transcriptomics
Study
EGAS00001003852
-
Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Study
EGAS00001001892
-
Transcriptome sequencing of gingivo-buccal oral squamous cell carcinoma for integrative analysis: alterations in expression of genes attributable to methylation changes
Study
EGAS00001003893
-
Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma.
Study
EGAS00001003895
-
Searching for variants associated with endometriosis
Study
EGAS00001001741
-
Whole genome and transcriptome analysis of anaplastic thyroid carcinoma
Study
EGAS00001001214
-
Germline MBD4 Mutations and Predisposition to Uveal Melanoma
Study
EGAS00001003941
-
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
Phenotypic_characterisation_of_LRRN4CL_over_expression
Study
EGAS00001003976
-
Sequencing data of multiple sarcoma samples for personalized medicine and endotype identification
Study
EGAS00001003981
-
Integrative_Oncogenomics_of_Multiple_Myeloma
Study
EGAS00001000036
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
Reconstruction of complex rearrangement patterns causing the initiation of clear cell renal cell carcinoma.
Study
EGAS00001004015
-
Molecular Attributes Underlying Central Nervous System and Systemic Relapse in Diffuse Large B-cell Lymphoma
Study
EGAS00001004057
-
Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission
Study
EGAS00001001973
-
Exome_sequencing_of_EBV_driven_lymphoma
Study
EGAS00001001021
-
Investigate the evolutionary trajectories during invasiveness acquisition in early lung adenocarcinoma
Study
EGAS00001004754
-
Phased whole genome sequencing of 10 melanoma samples
Study
EGAS00001004136
-
Metastatic Adult Pancreatoblastoma: Multimodal Treatment and Molecular Characterization of a Very Rare Disease (NCT MASTER)
Study
EGAS00001004157
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody
Study
EGAS00001004196
-
Immuno-genomic landscape of osteosarcoma
Study
EGAS00001004197
-
Pancreatic tropism of metastatic renal cell carcinoma
Study
EGAS00001004208
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
Mutation signatures in melanocytic nevi reveal characteristics of defective DNA repair
Study
EGAS00001004274
-
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Study
EGAS00001003493
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Mutational Landscape of Grey Zone Lymphoma
Study
EGAS00001004482
-
Transcriptomic analysis of the Phase 3 COMPARZ clinical trial
Study
EGAS00001004534
-
Targeted sequencing of Burkitt lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001004649
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
Evolutionary dynamics of residual disease in human glioblastoma
Study
EGAS00001003043
-
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
-
ChIP-seq of plasma cell-free nucleosomes identifies gene expression programs of the cells-of-origin
Study
EGAS00001004913
-
The Genetic Landscape of BCL2 Break Negative Follicular Lymphoma
Study
EGAS00001002164
-
WES used for direct identification of clinically relevant neoepitopes presented on native human melanoma tissue by mass spectrometry
Study
EGAS00001002050
-
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
-
Recurrent Somatic Mutations of PTPN1 in Primary Mediastinal B cell lymphoma and Hodgkin Lymphoma
Study
EGAS00001000554
-
Pediatric HGG WES and RNA-Seq
Study
EGAS00001005687