-
Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks
Study
EGAS00001002571
-
High Grade Serous Ovarian Carcinomas Originate in the Fallopian Tube
Study
EGAS00001002589
-
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
-
Employing_single_cell_sequencing_for_detection_of_mutational_signatures_reflecting_on_going_mutagenesis_
Study
EGAS00001002679
-
Chondromyxoid_fibroma
Study
EGAS00001000533
-
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
-
Gut microbiome modulates response to anti PD1 immunotherapy in metastatic melanoma patients
Study
EGAS00001002698
-
Germline alterations of acute myeloid leukemia
Study
EGAS00001002760
-
Whole exome and transcriptome sequencing of biliary tract cancer
Study
EGAS00001000950
-
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_2
Study
EGAS00001002372
-
Drug screening and whole genome sequencing of primary cells and cell lines from ovarian cancer patients to associate genomic aberrations with in vitro drug sensitivities
Study
EGAS00001002239
-
Genomic landscape of oral cancers (Illumina RNA-Seq)
Study
EGAS00001003237
-
EBV_AID_project
Study
EGAS00001000955
-
Genomic analysis Nasopharyngeal cancer through whole exome sequencing and whole genomic sequencing.
Study
EGAS00001002788
-
Prostate Cancer and Normal Adjacent Prostate RNA-seq samples, NGS-ProToCol
Study
EGAS00001002816
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS
Study
EGAS00001002858
-
Genome analysis of oesophageal cancer and Barrett's oesophagus
Study
EGAS00001002864
-
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
-
Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Study
EGAS00001002908
-
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
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
Whole-genome sequencing reveals genomic signatures associated with the inflammatory microenvironments in Chinese NSCLC patients
Study
EGAS00001002954
-
RNAseq___Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000813
-
Lung_Progression_versus_Regression_Whole_Genome_Sequencing
Study
EGAS00001000837
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Metastatic_Prostate_Follow_Up
Study
EGAS00001000730
-
Targeting the DNA Repair Pathway in Ewing Sarcoma
Study
EGAS00001000839
-
The molecular landscape of colorectal cancer (5 cases)
Study
EGAS00001002374
-
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
Study
EGAS00001003040
-
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
-
Oesophageal_Adenocarcinoma_Organoid_Hi_C
Study
EGAS00001003122
-
A comprehensive human gastric cancer organoid biobank captures tumor subtype heterogeneity and enables therapeutic screening
Study
EGAS00001003145
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas_LCM_
Study
EGAS00001003197
-
A Study to Evaluate Denosumab in Young Patients With Primary Breast Cancer (D-Beyond)
Study
EGAS00001003252
-
Enhanced detection of circulating tumor DNA by fragment size analysis
Study
EGAS00001003258
-
Molecular profiling of longitudinally observed small colorectal polyps: a cohort study
Study
EGAS00001003284
-
Chordoma_Extension__known_cancer_genes_
Study
EGAS00001000895
-
Adeno-associated virus in the liver: natural history and consequences in tumor development
Study
EGAS00001003310
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__BRCA_Carriers__Targeted_
Study
EGAS00001003315
-
Sequencing of liver cancer cell lines
Study
EGAS00001002237
-
The aim of this project is to identify, on 15 French Caucasian and 10 African-Caribbean men, through an integrative approach of DNA sequencing and transciptomic analyses, relevant genomic events that characterize or allow targeting the various phenotypes of aggressiveness of early stages of prostate cancer.
Study
EGAS00001002176
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Targeted_
Study
EGAS00001003318
-
Whole genome and RNA sequencing of paediatric glioblastoma in the ICGC PedBrain project
Study
EGAS00001001139
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Whole genome sequencing of Ewings Sarcoma
Study
EGAS00001003385
-
Utility of ctDNA to support patient selection for early phase clinical trials: The TARGET Study
Study
EGAS00001003407
-
Genetic Landscape of Esophageal Squamous Cell Carcinoma Defined by Exome Sequencing on Chinese Patient Cohort and Cell Lines
Study
EGAS00001000932
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
Myelodysplastic_Syndrome_Follow_Up_Series
Study
EGAS00001000224
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Study
EGAS00001003502
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___WG__Novaseq_
Study
EGAS00001003523
-
FFPE_whole_genome_pilot
Study
EGAS00001001967
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Study
EGAS00001000946
-
Evolution of GBM through therapy
Study
EGAS00001003546
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Pulldown_DNA_methylation_study_v2
Study
EGAS00001000979
-
This study explored and validated the clinical application of targeted NGS of circulating tumor DNA in identifying tumor-specific mutations and uncovering clinical actionable targets in a variety of solid tumors in large patient cohorts.
Study
EGAS00001002251
-
Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Study
EGAS00001003661
-
Multi-layered molecular characterization defines prognostic subtypes of lung adenocarcinoma in Asian never-smokers
Study
EGAS00001003705
-
Infant Glioma Molecular Subtype
Study
EGAS00001003714
-
SNU_PROSPECTIVE
Study
EGAS00001002154
-
RNAseq_of_patients_with_Ewings_sarcoma
Study
EGAS00001000267
-
Patient-Derived Lung Cancer Organoid
Study
EGAS00001003786
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET)
Study
EGAS00001003813
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
Organoid_Derivation_Project__TGS
Study
EGAS00001002221
-
Genomic analysis of HPV positive versus HPV negative esophageal adenocarcinoma
Study
EGAS00001001340
-
Fibroblast heterogeneity and immunosuppressive environment in Human breast cancer
Study
EGAS00001002508
-
WGS-Lung Cancer sample 30 pair
Study
EGAS00001001474
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
A Functional Network of Gastric-Cancer-Associated Splicing Events Controlled by Dysregulated Splicing Factors
Study
EGAS00001002256
-
Whole genome and transcriptome analysis of medullary thyroid cancer
Study
EGAS00001001473
-
Feasibility_of_targeted_capture_sequencing_in_FFPE_cancer_specimens_2
Study
EGAS00001000402
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Study
EGAS00001002257
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
-
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
-
Nuclear_single_seq_pilot
Study
EGAS00001003386
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
Ewings_Sarcoma_Rearrangement_Screen
Study
EGAS00001000362
-
71 Whole-exome sequencing of Esophageal Squamous Cell Carcinoma on Chinese Patients
Study
EGAS00001001475
-
Clonal_architecture_of_pre_malignant_and_malignant_tumours
Study
EGAS00001001676
-
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
-
Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas.
Study
EGAS00001002271
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
Whole-genome sequencing analysis of low-grade astrocytomas within the ICGC PedBrain Tumor Project
Study
EGAS00001000381
-
Single cell RNA sequencing and Whole Genome Sequencing on different cells from the same sample for a triple negative patient derived xenograft and ovarian cancer cell lines.
Study
EGAS00001003387
-
MDSMPN_Rearrangement_Screen
Study
EGAS00001000034
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
Benchmarking_CRISPR_Whole_genome_Drop_out_Screen___B_S
Study
EGAS00001002931
-
PREDICT
Study
EGAS00001000094