-
Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis
Study
EGAS00001000515
-
CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
-
Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Exome_
Study
EGAS00001003319
-
Distinct evolutionary trajectories of primary high grade serous ovarian cancers revealed through spatial mutational profiling
Study
EGAS00001000547
-
Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
Study
EGAS00001000565
-
Human_Developmental_Cell_Atlas_HDCA___WGS
Study
EGAS00001002929
-
Feasibility_of_targeted_capture_sequencing_in_routinely_collected_FFPE_cancer_specimens
Study
EGAS00001000297
-
RB1 Gene Inactivation by Chromothripsis in Human Retinoblastoma
Study
EGAS00001000598
-
Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability
Study
EGAS00001000599
-
Whole exome sequencing of papillary thyroid carcinoma in the Chinese population
Study
EGAS00001001268
-
Sequencing_of_rare_human_histiocytic_tumour
Study
EGAS00001000591
-
Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis_PART2
Study
EGAS00001000603
-
The molecular landscape of colorectal cancer (17 cases)
Study
EGAS00001002174
-
T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases
Study
EGAS00001007136
-
Osteosarcoma_RNAseq
Study
EGAS00001000615
-
Neoadjuvant_Breast_Cancer_Validations
Study
EGAS00001000428
-
BAP1_sequence_of_uveal_melanoma_cell_lines
Study
EGAS00001001520
-
Developing somatic copy number and mutation calling tools for a bespoke sequencing platform
Study
EGAS00001007195
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Genome-wide sequencing of (cell-free) DNA from Nipple aspirate fluid of Breast cancer patients
Study
EGAS00001007214
-
MPN_mutation_order_followup
Study
EGAS00001000663
-
Breast_Heterogeneity_Validation
Study
EGAS00001001972
-
Single Cell RNAseq of blood and tumor from renal cancer patients
Study
EGAS00001004230
-
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
-
TRACERx 100: RNAseq data from the first 100 TRACERx tumours
Study
EGAS00001003458
-
Breast_Cancer_Matched_Pair_Cell_Line_Whole_Genomes
Study
EGAS00001000166
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Study
EGAS00001000650
-
Mutational_Signatures_of_relapse_in_rectal_cancer_FFPE_samples_in_the_CR07_clinical_trial
Study
EGAS00001000651
-
Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Study
EGAS00001007248
-
Exomes of High-risk Prostate cancer
Study
EGAS00001001015
-
CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
-
Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data
Study
EGAS00001000659
-
BASIS_RNAseq
Study
EGAS00001000707
-
Radiotherapy_induced_Sarcoma_exome
Study
EGAS00001000194
-
White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer
Study
EGAS00001004114
-
Whole exome sequencing of 103 pairs BLCA-CN
Study
EGAS00001000677
-
Inferring expressed genes by whole-genome sequencing of plasma DNA
Study
EGAS00001001754
-
GENOMIC INSTABILITY IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER
Study
EGAS00001002477
-
Metastatic_breast_cancer_targeted_gene_screen
Study
EGAS00001000704
-
Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004232
-
Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
Study
EGAS00001003530
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Study
EGAS00001000714
-
Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
-
Analysis of Loose Ends in Cancer Genome Structure
Study
EGAS00001007324
-
Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
-
Genome-wide cell-free DNA fragmentation in patients with cancer
Study
EGAS00001003611
-
Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines.
Study
EGAS00001000736
-
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Study
EGAS00001000738
-
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
-
Mesothelioma_Whole_Genomes
Study
EGAS00001000830
-
CGP_CORE_CELL_LINES___RNA_seq
Study
EGAS00001000828
-
2017_AML_WGS
Study
EGAS00001002388
-
Systems biology of Colorectal Cancer
Study
EGAS00001000854
-
RNA-sequençing of 21 inflammatory hepatocellular adenomas
Study
EGAS00001003685
-
Myeloma_Targeted_Follow_up_Study
Study
EGAS00001000880
-
Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer
Study
EGAS00001000882
-
Tracking the origins and drivers of subclonal metastatic expansion in prostate cancer
Study
EGAS00001000942
-
Y_chromosome_mis_segregation_in_the_DLD_1_cell_line
Study
EGAS00001002551
-
Single_Cell_Targeted_Sequence_Capture
Study
EGAS00001000435
-
B Cell Receptor Study From Metastatic Breast Cancer Tumour Samples
Study
EGAS00001006976
-
Origins and functional consequence of somatic mitochondrial DNA mutations
Study
EGAS00001000968
-
Angiosarcoma_whole_exome
Study
EGAS00001000588
-
Preclinical_evolution_of_haematological_malignancies_
Study
EGAS00001002128
-
HSC_population_dynamics___LEUK4_samples
Study
EGAS00001004247
-
Sequencing of serial plasma and multiregional tumor samples in a patient with metastatic breast cancer
Study
EGAS00001001466
-
Copy numbers in resectable gastric cancer treated with surgery alone
Study
EGAS00001007394
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Cell_Line_Sub_Clone_Rearrangement_Screen
Study
EGAS00001000178
-
Identification_of_drug_resistance_genes_in_cancer_cell_lines_by_insertional_mutagenesis
Study
EGAS00001001035
-
Fixative optimisation study for BRITROC project
Study
EGAS00001001433
-
Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
Study
EGAS00001003822
-
Finnish_population_cohort_genotyping_B
Study
EGAS00001001047
-
Translation of non-canonical open reading frames as a cancer cell survival mechanism in childhood medulloblastoma
Study
EGAS00001007426
-
Comparison of HCC cell lines and primary HCCs
Study
EGAS00001001678
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
-
Transcriptome sequencing of gingivo-buccal oral squamous cell carcinoma for integrative analysis: alterations in expression of genes attributable to methylation changes
Study
EGAS00001003893
-
Metastatic_Prostate_Follow_Up
Study
EGAS00001000730
-
Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Study
EGAS00001003928
-
MiR expression profiles of paired primary colorectal cancerand metastases by next-generation sequencing
Study
EGAS00001001127
-
SNU_WGS_AML
Study
EGAS00001001906
-
Multiple_Malignancy_Familial_Comparison
Study
EGAS00001000333
-
Rapid identification of somatic genome rearrangements as personalized biomarkers for blood-based cancer monitoring
Study
EGAS00001003963
-
Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation
Study
EGAS00001001940
-
Integrative_Oncogenomics_of_Multiple_Myeloma
Study
EGAS00001000036
-
Wilms_Tumour_organoid_sequencing_WGS
Study
EGAS00001002692
-
Reconstruction of complex rearrangement patterns causing the initiation of clear cell renal cell carcinoma.
Study
EGAS00001004015
-
RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines.
Study
EGAS00001000610
-
CLL_targeted_exome_sequencing
Study
EGAS00001001963
-
Exome_sequencing_of_EBV_driven_lymphoma
Study
EGAS00001001021
-
Detection of Gene Fusions using Targeted Next-Generation Sequencing – a Comparative Evaluation
Study
EGAS00001004934
-
Whole exome sequencing of advanced gastric cancer
Study
EGAS00001004086
-
Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
Study
EGAS00001004093
-
Organoid_Derivation_Pilot__RNAseq
Study
EGAS00001002223