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Angiosarcoma_follow_up_study
Study
EGAS00001000405
-
Orphan_Tumour_Study___familial_neuroblastoma
Study
EGAS00001002171
-
Integrated Molecular Profilting in Advanced Cancers Trial
Study
EGAS00001001897
-
WES of 2 human osteosarcoma and corresponding cell lines
Study
EGAS00001003923
-
BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs
Study
EGAS00001002298
-
Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Study
EGAS00001002326
-
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
-
Leiden_melanomafamilies
Study
EGAS00001000627
-
Chondrosarcoma_Exome_
Study
EGAS00001000038
-
ICGC medulloblastoma whole genome sequencing data, ICGC release 16
Study
EGAS00001000744
-
Chordoma_Extension_Study
Study
EGAS00001000892
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Anaplastic_Meningioma_V3__cancer_gene_panel
Study
EGAS00001001155
-
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
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 1).
Study
EGAS00001002630
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
-
Aggressive genomic features in clinicallyindolent primary HHV8-negative effusion-based lymphoma
Study
EGAS00001002743
-
Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma
Study
EGAS00001004076
-
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
2014_Lung_sq_WES
Study
EGAS00001002844
-
Patients with metastatic urothelial carcinoma
Study
EGAS00001002114
-
Targeted_analysis_of_chondrosarcoma_cancer_genes
Study
EGAS00001001765
-
The_genomic_architecture_of_mesothelioma_
Study
EGAS00001000353
-
Diverse modes of genomic alterations in hepatocellular carcinoma
Study
EGAS00001000824
-
ChIP-seq data of Hodgkin lymphoma cell line L-428
Study
EGAS00001003033
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
Osteosarcoma_X10
Study
EGAS00001002167
-
Burden_of_Disease_in_Sarcoma
Study
EGAS00001000087
-
The molecular landscape of glioma in patients with Neurofibromatosis 1.
Study
EGAS00001003186
-
ICGC Oesophageal adenocarcinoma - lymph-node samples
Study
EGAS00001000727
-
Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma.
Study
EGAS00001002501
-
Comprehensive miRNA Sequence Analysis Reveals Survival Differences in Diffuse Large B-cell Lymphoma Patients
Study
EGAS00001001025
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA.
Study
EGAS00001001147
-
MGA-NUTM1 fusion in high grade spindle cell sarcoma
Study
EGAS00001003341
-
Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
-
Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
Study
EGAS00001000565
-
Uveal melanoma patient with germline MBD4 nonsense mutation
Study
EGAS00001003362
-
Deciphering the mutational landscape and the genome organization of LMS
Study
EGAS00001001262
-
Genomic and transcriptomic profiling of signalling networks in follicular lymphoma
Study
EGAS00001002175
-
Whole exome sequencing of papillary thyroid carcinoma in the Chinese population
Study
EGAS00001001268
-
Osteosarcoma_RNAseq
Study
EGAS00001000615
-
BAP1_sequence_of_uveal_melanoma_cell_lines
Study
EGAS00001001520
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Mutational_Signatures_of_relapse_in_rectal_cancer_FFPE_samples_in_the_CR07_clinical_trial
Study
EGAS00001000651
-
CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
-
Integrative genomic profiling of hepatocellular adenomas reveals recurrent FRK activating mutations and mutational processes of malignant transformation
Study
EGAS00001000679
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
-
Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
-
Mesothelioma_Whole_Genomes
Study
EGAS00001000830
-
Study of pediatric hepatocellular carcinoma caused by bile salt export pump deficiency
Study
EGAS00001000749
-
Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
-
Human_primary_melanoma_project
Study
EGAS00001002409
-
Angiosarcoma_whole_exome
Study
EGAS00001000588
-
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
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Modeling glioblastoma invasion using human brain organoids and single-cell transcriptomics
Study
EGAS00001003852
-
Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma.
Study
EGAS00001003895
-
Whole genome and transcriptome analysis of anaplastic thyroid carcinoma
Study
EGAS00001001214
-
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
-
Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
-
Integrative_Oncogenomics_of_Multiple_Myeloma
Study
EGAS00001000036
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
Molecular Attributes Underlying Central Nervous System and Systemic Relapse in Diffuse Large B-cell Lymphoma
Study
EGAS00001004057
-
Reconstruction of complex rearrangement patterns causing the initiation of clear cell renal cell carcinoma.
Study
EGAS00001004015
-
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
-
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
-
Pancreatic tropism of metastatic renal cell carcinoma
Study
EGAS00001004208
-
Mutation signatures in melanocytic nevi reveal characteristics of defective DNA repair
Study
EGAS00001004274
-
Investigate the evolutionary trajectories during invasiveness acquisition in early lung adenocarcinoma
Study
EGAS00001004754
-
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
-
Evolutionary dynamics of residual disease in human glioblastoma
Study
EGAS00001003043
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
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
-
Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
-
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Study
EGAS00001003493
-
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
-
PLCG1 R707Q mutation is counter selected under targeted therapy in a patient with a hepatic angiosarcoma
Study
EGAS00001001281
-
Transcriptional mechanisms of resistance to anti-PD-1 therapy
Study
EGAS00001002195
-
Circumventing intratumoral heterogeneity to identify potential therapeutic targets in hepatocellular carcinoma. Details please contact lifuqiang@genomics and zhaoxin@genomics.cn.
Study
EGAS00001002207
-
Angiosarcoma_RNA_sequencing
Study
EGAS00001000590
-
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Study
EGAS00001002337
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
Cell motility and migration as determinants of stem cell efficacy
Study
EGAS00001002478