-
Genomic study of an AT-AML
Study
EGAS00001004392
-
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Lung cohort
Study
EGAS00001004447
-
Whole exome sequencing of long-term, never relapse exceptional responders of trastuzumab-treated HER2+ metastatic breast cancer
Study
EGAS00001004486
-
RNA-seq data from 121 tumor samples with muscle invasive bladder cancer.
Study
EGAS00001004505
-
Chromosomal copy number heterogeneity predicts survival rates across cancers
Study
EGAS00001004702
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
-
Angiosarcoma_follow_up_study
Study
EGAS00001000405
-
Mutational signatures in head and neck cancer (H019)
Study
EGAS00001004588
-
Molecular sub-classification of hormone receptor-positive breast cancer
Study
EGAS00001004594
-
Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing
Study
EGAS00001000566
-
whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
-
In this study, we performed exon sequencing (WXS) of 80 paired Brain cancer tumors and adjacent normal tissues to identify novel potential biomarkers. We extracted mutational signatures which induce somatic mutations . Our study covers a comprehensive genetic framework that can be used in clinical trials and treatment modalities in Brain cancer.
Study
EGAS00001002352
-
CEHM
Study
EGAS00001002366
-
Genomic analysis of patient-derived xenograft models reveals intratumor-heterogeneity in endometrial cancer and can predict tumor growth inhibition with talazoparib
Study
EGAS00001004666
-
Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
-
Field_effect_of_healthy_and_diseased_livers
Study
EGAS00001002382
-
Low_Coverage_Sequencing_of_rare_human_histiocytic_tumour
Study
EGAS00001000768
-
Immunological hallmarks for clinical response to BCG in bladder cancer
Study
EGAS00001004764
-
ENCORE__New_Targets_for_Effective_Combination_Therapies_in_Tumors_with_Unmet_Medical_Need
Study
EGAS00001004775
-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
Myeloma_Follow_up_Pilot
Study
EGAS00001000743
-
WGS___Mutant_clone_mapping_in_normal_oesohagus_and_skin
Study
EGAS00001002416
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
Chordoma_Extension_Study
Study
EGAS00001000892
-
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
-
Subclonal evolution of four ER+ breast cancers determined by WGS and scRNA-Seq
Study
EGAS00001002436
-
Transcriptional profiling of ovarian tumours and cell lines
Study
EGAS00001004814
-
Long-read and short-read isoform sequencing in breast cancer
Study
EGAS00001004819
-
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
-
Clonal_architecture_of_pre_malignant_and_malignant_tumours
Study
EGAS00001001676
-
Assessment of genomic copy number alterations in breast cancer
Study
EGAS00001000585
-
RNAseq_of_ribosomal_footprints
Study
EGAS00001001591
-
Inter and intra - tumor heterogeneity in Colorectal Cancer
Study
EGAS00001002150
-
Similarity and diversity of the tumor microenvironment in multiple metastases: critical implications for overall and progression-free survival of high-grade serous ovarian cancer.
Study
EGAS00001002065
-
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
-
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
-
Whole Genomes Define Concordance in Matched Primary, Xenograft, and Organoid Models of Pancreas Cancer
Study
EGAS00001002597
-
The Ovarian Cancer Association Consortium OncoArray genome-wide association study
Study
EGAS00001002305
-
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Study
EGAS00001002329
-
Molecular subtypes of malignant peritoneal mesothelioma
Study
EGAS00001002820
-
Pharmacogenomic landscape of patient-derived cells informs precision oncology therapy
Study
EGAS00001002515
-
Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
Y_chromosome_mis_segregation_in_the_DLD_1_cell_line
Study
EGAS00001002551
-
ChIP_sequencing_in_Cancer_Cell_Lines
Study
EGAS00001000203
-
Targeted_analysis_of_chondrosarcoma_cancer_genes
Study
EGAS00001001765
-
Genome-wide DNA Copy Number Analysis of high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001007049
-
Exome-wide somatic mutation characterization of small bowel adenocarcinoma
Study
EGAS00001002559
-
High-grade serous ovarian cancer refined with single-cell RNA-sequencing
Study
EGAS00001004987
-
Comparative genomics research for Chinese colorectal cancer
Study
EGAS00001002576
-
Direct Detection of Early-stage Cancers Using Circulating Tumor DNA
Study
EGAS00001002577
-
Colorectal_organoids_and_tumour_tissue
Study
EGAS00001000881
-
Melanoma_C32_ENU_resistance_to_Combination_Therapy
Study
EGAS00001001614
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas
Study
EGAS00001002533
-
Combination Therapies for Personalised Cancer Medicine in 11-18
Study
EGAS00001002579
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
Systematic kinase inhibitor profiling identifies CDK9 as a synthetic lethal target in NUT midline carcinoma
Study
EGAS00001002588
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 1).
Study
EGAS00001002630
-
V2_Colorectal_panel_test
Study
EGAS00001001806
-
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Study
EGAS00001002646
-
OCCAMS_Oesophageal_Cancer_Organoids_1
Study
EGAS00001001382
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
WGS of 32 paired SRCC samples
Study
EGAS00001002668
-
MicroRNA expression in malignant and benign breast tissue – the Norwegian Women and Cancer study
Study
EGAS00001002671
-
Employing_single_cell_sequencing_for_detection_of_mutational_signatures_reflecting_on_going_mutagenesis_
Study
EGAS00001002679
-
Dynamics of neoantigen landscape during immunotherapy
Study
EGAS00001002704
-
WGS___Exploration_of__mutational_processes_in_human_cancer_cell_lines
Study
EGAS00001002680
-
Gut microbiome modulates response to anti PD1 immunotherapy in metastatic melanoma patients
Study
EGAS00001002698
-
CD8+ Tumor-Infiltrating Lymphocyte Abundance is a Positive Prognostic Indicator in Nasopharyngeal Cancer
Study
EGAS00001006396
-
CancerDetector: Ultrasensitive and Non-Invasive Cancer Detection at the Resolution of Individual Reads using Cell-free DNA Methylation Sequencing Data
Study
EGAS00001002728
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Genomic analysis of Japanese gastric cancer (345 gastric cancers of NCC)
Study
EGAS00001002884
-
ALK_inhibitors_in_the_context_of_ALK_dependent_cancer_cell_lines
Study
EGAS00001000082
-
Cancer sequencing for somatic variant calling
Study
EGAS00001007101
-
Myelodysplastic_Syndrome_Exome_Sequnecing
Study
EGAS00001000089
-
Colorectal adenomas and carcinomas NKI-AvL TGO series Gut2009
Study
EGAS00001002758
-
Comparison of HCC cell lines and primary HCCs
Study
EGAS00001001678
-
LICA-CN project - 116 liver cancer cases
Study
EGAS00001002300
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 2).
Study
EGAS00001002771
-
GBM cancer stem cell lines -RNA-seq and WGS data
Study
EGAS00001003700
-
ER___HER2___PR__breast_Cancer_genome_sequencing
Study
EGAS00001000197
-
Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing)
Study
EGAS00001002784
-
DERMATLAS__Tubular_adenoma
Study
EGAS00001006686
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
V4_panel_bait_design_test
Study
EGAS00001001808
-
Familial_Thrombocytosis_germline_exome_sequencing
Study
EGAS00001000088
-
Feasibility_of_targeted_capture_sequencing_in_routinely_collected_FFPE_cancer_specimens
Study
EGAS00001000297
-
Breast cancer DNA repair
Study
EGAS00001002792
-
The molecular landscape of homologous recombination deficient, end-stage, high grade serous ovarian cancer
Study
EGAS00001006789
-
Neoadjuvant_Breast_Cancer_Validations
Study
EGAS00001000428
-
Genome analysis of oesophageal cancer and Barrett's oesophagus
Study
EGAS00001002864
-
Clonal_haematopoiesis_in_patients_with_AAA
Study
EGAS00001002873
-
Chordoma_Extension__known_cancer_genes_
Study
EGAS00001000895
-
Colorectal_organoids_and_tumoroids___pulldown
Study
EGAS00001000869
-
MPN_mutation_order_followup
Study
EGAS00001000663
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136