-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Study
EGAS00001007045
-
Genome-wide DNA Copy Number Analysis of high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001007049
-
Treatment stratification and biomarker validation using patient-derived head and neck cancer organoids
Study
EGAS00001007076
-
Cell-to-cell variability in Myc dynamics drives transcriptional heterogeneity in cancer cells
Study
EGAS00001007091
-
Long-term organoid culture of a small intestinal neuroendocrine tumor
Study
EGAS00001007093
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Cancer sequencing for somatic variant calling
Study
EGAS00001007101
-
Genomic profiling of Rare Tumors
Study
EGAS00001007103
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
Establishment and characterization of an Epstein-Barr virus-positive cell line from a non-keratinizing differentiated primary nasopharyngeal carcinoma
Study
EGAS00001007172
-
T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases
Study
EGAS00001007136
-
Persister cell phenotypes contribute to poor patient outcomes after neoadjuvant chemotherapy in PDAC (Hipo_015)
Study
EGAS00001007143
-
Molecular analysis of cancer genomes in children with Lynch syndrome: exploring causal associations
Study
EGAS00001007146
-
Human lymphoma plasma cfRNA - raw data
Study
EGAS00001007127
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
Enhanced detection of MRD with cfDNA Fragmentomics.
Study
EGAS00001007192
-
Cachexia - Non-Cachexia Metagenome Analysis
Study
EGAS00001007156
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00000000052
-
Breast Cancer Follow Up Series
Study
EGAS00001000002
-
Multifocal_Breast_Project
Study
EGAS00001000004
-
Chondrosarcoma_Exome_
Study
EGAS00001000038
-
Kaposi_sarcoma_exome
Study
EGAS00001000032
-
1__Fanconi_Anemia_transformation_to_AML
Study
EGAS00001000033
-
Lung_Cancer_Whole_Genomes
Study
EGAS00001000148
-
ALK_inhibitors_in_the_context_of_ALK_dependent_cancer_cell_lines
Study
EGAS00001000082
-
Linking genes, genomic instability and molecular subgroups in medulloblastoma
Study
EGAS00001000085
-
Familial_Thrombocytosis_germline_exome_sequencing
Study
EGAS00001000088
-
PREDICT
Study
EGAS00001000094
-
Cell_Line_Sub_Clone_Rearrangement_Screen
Study
EGAS00001000178
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000199
-
Splenic_Marginal_Zone_Lymphoma_with_villous_lymphocytes_exome_sequencing
Study
EGAS00001000139
-
an integrated molecular study of clear cell renal cell carcinoma (ccRCC) including whole-genome/exome and RNA sequencing as well as array-based gene expression/copy-number/methylation analyses
Study
EGAS00001000509
-
BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
-
Chordoma_Exome_Sequencing
Study
EGAS00001000188
-
ADCC_Exome_Sequencing
Study
EGAS00001000193
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00001000245
-
Single-cell RNA-seq data from metastatic ovarian cancer for quality control study
Study
EGAS00001005066
-
Chondrosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000277
-
AML_targeted_resequencing_study
Study
EGAS00001000275
-
Pancreatic Cancer Sequencing Initiative
Study
EGAS00001000343
-
Triple_Negative_Breast_Cancer_Whole_Genome_Validations
Study
EGAS00001000426
-
Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Study
EGAS00001000490
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Spatial Transcriptomics on prostate cancer heterogeneity
Study
EGAS00001003001
-
Discovery of cancer prognostic markers based on comparison of gene expression in colorectal cancer samples.
Study
EGAS00001005068
-
Targeted_sequencing_of_genes_recurrently_mutated_in_AML___part2
Study
EGAS00001000570
-
Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis_PART2
Study
EGAS00001000603
-
Mosaic_Colorectal_Metastasis
Study
EGAS00001000613
-
BIG_MS_Pilot
Study
EGAS00001000616
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
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
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Study
EGAS00001000714
-
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
-
Exploration_of__mutational_processes_in_human_cancer_cell_lines__Exome
Study
EGAS00001000790
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Deep_sequencing_of_melanoma_for_driver_mutations
Study
EGAS00001000857
-
Intra-tumor heterogeneity of localized lung adenocarcinomas defined by multi-region sequencing
Study
EGAS00001000930
-
Whole genome study of Hurthle cell thyroid carcinoma
Study
EGAS00001000940
-
Persistence of circulating tumor DNA in breast cancer patients during neoadjuvant treatment is a significant predictor of poor tumor response
Study
EGAS00001005798
-
WGS and WES of 78 pairs Chinese gastric cancer
Study
EGAS00001001056
-
Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Study
EGAS00001005812
-
Germline alterations of acute myeloid leukemia
Study
EGAS00001002760
-
CONSERTING: integrating copy number analysis with structural variation detection
Study
EGAS00001001202
-
Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells
Study
EGAS00001001310
-
The genomic and radiomic complexity of multifocal prostate cancer
Study
EGAS00001002767
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
Whole genome and transcriptome analysis of medullary thyroid cancer
Study
EGAS00001001473
-
Transcriptome profiling for Korean Diffuse Gastric cancers
Study
EGAS00001001859
-
Clonal_expansion_of_mutated_cell_population_in_bladder_urothelium_
Study
EGAS00001001687
-
ENU_NCI_H508_cetuximab_fixed_concentration_project
Study
EGAS00001001744
-
Tumor-intrinsic expression of the autophagy gene Atg16l1 suppresses anti-tumor immunity in colorectal cancer
Study
EGAS00001005952
-
Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Study
EGAS00001001782
-
Spiradenocarcinoma
Study
EGAS00001001799
-
Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility
Study
EGAS00001001789
-
Detection of Gene Fusions using Targeted Next-Generation Sequencing – a Comparative Evaluation
Study
EGAS00001004934
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies unique proteotypes associated with patient outcomes
Study
EGAS00001006068
-
A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (normal data)
Study
EGAS00001006098
-
Genetic immune escape landscape in primary and metastatic cancer
Study
EGAS00001006123
-
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
-
BGISEQ-500 Cancer Dataset - WGS tumour/normal pairs
Study
EGAS00001002298
-
2017_AML_WGS
Study
EGAS00001002388
-
18 Whole Exome Sequencing for Radiation Induced-Meningiomas
Study
EGAS00001002317
-
RNA seq on 19 samples of Radiation-Induced Meningiomas
Study
EGAS00001002318
-
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
-
H3K27ac ChIP-seq in TMPRSS2:ERG positive and negative prostate cancer tissue samples
Study
EGAS00001002496
-
Combination Therapies for Personalised Cancer Medicine in drug resistant EGFR mutant lung cancer
Study
EGAS00001002509
-
Comparative genomics research for Chinese colorectal cancer
Study
EGAS00001002607
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma
Study
EGAS00001002608
-
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
-
Breast cancer women lack normal lifelong immune response after full-term pregnancies
Study
EGAS00001002616
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WGS
Study
EGAS00001002658
-
WGS___Exploration_of__mutational_processes_in_human_cancer_cell_lines
Study
EGAS00001002680
-
Keratinocyte_CRISPR_screens
Study
EGAS00001002714
-
Shallow nanopore RNA sequencing enables transcriptome profiling for precision cancer medicine (Hipo_021)
Study
EGAS00001006317