-
Comprehensive molecular profiling identifies novel genetic drivers and subtypes underlying medulloblastoma
Study
EGAS00001001953
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Study
EGAS00001000714
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102
-
Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Study
EGAS00001000737
-
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Study
EGAS00001000761
-
EBV_AID_project
Study
EGAS00001000955
-
MYC Drives Progression of Small Cell Lung Cancer to a Variant Neuroendocrine Subtype with Vulnerability to Aurora Kinase Inhibition
Study
EGAS00001002115
-
Exploration_of__mutational_processes_in_human_cancer_cell_lines__Exome
Study
EGAS00001000790
-
Xenograft_Sequencing
Study
EGAS00001000140
-
Identification_of_synthetic_lethal_genes_by_CRISPR_Cas9_library
Study
EGAS00001002117
-
Osteosarcoma_Whole_Genome
Study
EGAS00001000147
-
Exomes of High-risk Prostate cancer
Study
EGAS00001001015
-
Preclinical_evolution_of_haematological_malignancies_
Study
EGAS00001002128
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR
Study
EGAS00001002132
-
Two lung cancer cell lines with EGFR mutations, PC-9 and KHM-3S, were either treated with Tarceva for 24 hours or left untreated. The gene expression profiles were examined by RNAseq, and the genome wide binding profiles of total STAT3 and pSTAT3 were characterized by ChIPseq.
Study
EGAS00001000793
-
RNAseq___Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000813
-
Inter and intra - tumor heterogeneity in Colorectal Cancer
Study
EGAS00001002150
-
Lung_Progression_versus_Regression_Whole_Genome_Sequencing
Study
EGAS00001000837
-
Targeting the DNA Repair Pathway in Ewing Sarcoma
Study
EGAS00001000839
-
Metastatic_Prostate_Follow_Up_2
Study
EGAS00001000756
-
Genomics_of_Colorectal_Cancer_Metastases___Massively_Parallel_Sequencing_of_Matched_Primary_and_Metastatic_tumours_to_Identify_a_Metastatic_Signature_of_Somatic_Mutations__MOSAIC_
Study
EGAS00001000103
-
Balanced_Ependymoma
Study
EGAS00001000174
-
Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine
Study
EGAS00001000853
-
Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer
Study
EGAS00001000882
-
Chordoma_Extension__known_cancer_genes_
Study
EGAS00001000895
-
miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
-
Whole genome and RNA sequencing of paediatric glioblastoma in the ICGC PedBrain project
Study
EGAS00001001139
-
AML_WES
Study
EGAS00001001559
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines
Study
EGAS00001000932
-
Myelodysplastic_Syndrome_Follow_Up_Series
Study
EGAS00001000224
-
FFPE_whole_genome_pilot
Study
EGAS00001001967
-
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Study
EGAS00001000946
-
Pulldown_DNA_methylation_study_v2
Study
EGAS00001000979
-
SNU_PROSPECTIVE
Study
EGAS00001002154
-
Finnish_population_cohort_genotyping_B
Study
EGAS00001001047
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
RNAseq_of_patients_with_Ewings_sarcoma
Study
EGAS00001000267
-
WGS-Lung Cancer sample 30 pair
Study
EGAS00001001474
-
Genomic analysis of HPV positive versus HPV negative esophageal adenocarcinoma
Study
EGAS00001001340
-
Melanoma_multi_site_metastases
Study
EGAS00001001348
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
Whole genome and transcriptome analysis of medullary thyroid cancer
Study
EGAS00001001473
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
-
71 Whole-exome sequencing of Esophageal Squamous Cell Carcinoma on Chinese Patients
Study
EGAS00001001475
-
Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Ewings_Sarcoma_Rearrangement_Screen
Study
EGAS00001000362
-
Mutational_Analysis_of_Colorectal_PDX_models
Study
EGAS00001001171
-
Clonal_architecture_of_pre_malignant_and_malignant_tumours
Study
EGAS00001001676
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Whole genome sequencing and whole exome sequencing of DIPG tumors and matched normal tissue
Study
EGAS00001000575
-
Angiosarcoma_targeted_pulldown_cancer_gene_panel
Study
EGAS00001000589
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
Evaluation_of_size_selection_on_cancer_specific_sequencing_libraries
Study
EGAS00001000293
-
Whole-genome sequencing analysis of low-grade astrocytomas within the ICGC PedBrain Tumor Project
Study
EGAS00001000381
-
Tissue-specific mutation accumulation in human adult stem cells during life
Study
EGAS00001001682
-
MDSMPN_Rearrangement_Screen
Study
EGAS00001000034
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
Feasibility_of_targeted_capture_sequencing_in_FFPE_cancer_specimens_2
Study
EGAS00001000402
-
PREDICT
Study
EGAS00001000094
-
Comparing nodal versus bony metastatic spread using tumour phylogenies
Study
EGAS00001001801
-
Mixed_Leukemia_Rearrangement_Screen
Study
EGAS00001000180
-
Interactions between the tumor and the systemic response of breast cancer patients
Study
EGAS00001001804
-
Acute_Lymphoblastic_Leukemia_Exome_sequencing
Study
EGAS00001000201
-
Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Study
EGAS00001000255
-
Molecular evolution of metastatic clear cell renal cell carcinoma progressing under tyrosine kinase inhibitor therapy (HIPO-045)
Study
EGAS00001001861
-
Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies
Study
EGAS00001000274
-
CML_Discovery_Project
Study
EGAS00001000218
-
Chordoma_Targeted_Sequencing_Study
Study
EGAS00001000280
-
Mutant_clone_mapping_in_normal_oesophagus
Study
EGAS00001001874
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
Single cell Transcriptomic Analysis of Cellular Heterogeneity in Human Colorectal Tumors
Study
EGAS00001001945
-
Cancer_Cell_Line_Exome_Sequencing_
Study
EGAS00001000978
-
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_
Study
EGAS00001001941
-
Chordoma_Sequencing_Project_RNAseq
Study
EGAS00001000410
-
Breast_Cancer_FRT_RNA_seq
Study
EGAS00001000420
-
Breast_cancer_sequential_sampling_study
Study
EGAS00001000300
-
Pseudogene_RNAseq
Study
EGAS00001000606
-
Plasma-Seq of patients with metastatic prostate cancer
Study
EGAS00001000451
-
Whole genome and transcriptome analysis of a sporadic and recurring parathyroid carcinoma
Study
EGAS00001000484
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
Study
EGAS00001000565
-
Osteosarcoma_X10
Study
EGAS00001002167
-
RB1 Gene Inactivation by Chromothripsis in Human Retinoblastoma
Study
EGAS00001000598
-
The molecular landscape of colorectal cancer (17 cases)
Study
EGAS00001002174
-
Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
-
Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers
Study
EGAS00001000621
-
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
TMD_AMKL_targeted_follow_up_part_2
Study
EGAS00001000732
-
MPN_TGS2_Follow_up___PT1_Vori_other
Study
EGAS00001000765
-
CMF_RNA_sequencing
Study
EGAS00001000470
-
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
-
Chondromyxoid_fibroma
Study
EGAS00001000533
-
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
-
Targeted_gene_screen_of_drug_resistant_organoids
Study
EGAS00001001797