-
Molecular analysis of post-colonoscopy CRC (PCCRC)
Study
EGAS00001004686
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Study
EGAS00001003536
-
To_profile_the_landscape_of_sebaceous_tumours_WES
Study
EGAS00001003553
-
Amplicon_based_sequencing_of_drug_resistant_lung_cancer_cell_lines
Study
EGAS00001001675
-
Cancer-Associated Mutations in Endometriosis without Cancer
Study
EGAS00001003576
-
Multi-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors
Study
EGAS00001001871
-
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
-
Chromosomal copy number heterogeneity predicts survival rates across cancers
Study
EGAS00001004702
-
Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells
Study
EGAS00001001310
-
ENU_LS_411N_TripleTherapy
Study
EGAS00001001777
-
ENU_HT_29_BRAF_Triple_Therapy_Clones
Study
EGAS00001001778
-
Enrichment of homologous recombination repair alteration in prostate cancer brain metastases
Study
EGAS00001005091
-
The clonal and mutational evolution spectrum of primary triple negative breast cancers
Study
EGAS00001000132
-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
-
A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
-
Breast Cancer - Subtype defined by an amplification of the HER2 gene
Study
EGAS00001001431
-
Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
-
Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency
Study
EGAS00001000149
-
Glioblastoma_CRISPR_Screen
Study
EGAS00001001519
-
A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Study
EGAS00001001539
-
Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
-
The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer
Study
EGAS00001001573
-
Rucaparib in patients presenting a metastatic breast cancer with Homologous Recombination Deficiency, without germline BRCA1/2 mutation, pronostic value of high LOH genomic score and predictive value of HRDetect (microarray)
Study
EGAS00001004755
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
-
In_Situ_Transcription_whole_genome_sequencing
Study
EGAS00001001971
-
FRCC_Exome_sequencing
Study
EGAS00001000176
-
Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Study
EGAS00001003620
-
Signatures of mismatch repair deficiency in cancer genomes
Study
EGAS00001000182
-
CML_blast_phase_rearrangement_screen
Study
EGAS00001000191
-
SCAT_osteosarcoma_sequencing
Study
EGAS00001000196
-
RNASeq of PDX and CDX tumours treated with ADC
Study
EGAS00001004562
-
Mutations conferring differential treatment response in breast cancer
Study
EGAS00001003626
-
Whole genome, transcriptome and methylome profiling enhances actionable target discovery in high-risk paediatric cancer
Study
EGAS00001004572
-
Non_Tumour_Renal_Cell_Line_Sequencing
Study
EGAS00001000205
-
Cancer_Genome_Libraries_Tests
Study
EGAS00001000208
-
Test_of_PCR_library_method_on_whole_genmoe_samples
Study
EGAS00001000214
-
Multi-omics Profiling of Asian Breast Cancers
Study
EGAS00001002621
-
Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
-
Warm_Autopsy_Single_Cell_X10
Study
EGAS00001001698
-
Identifying_Novel_Fusion_Genes_in_Myeloma
Study
EGAS00001000220
-
Mutational signatures in head and neck cancer (H019)
Study
EGAS00001004588
-
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
-
Paediatric_CNS_tumour_autopsy_DNA
Study
EGAS00001004771
-
Breast Cancer - immune clusters - RNA-seq
Study
EGAS00001003631
-
Molecular sub-classification of hormone receptor-positive breast cancer
Study
EGAS00001004594
-
ENCORE__New_Targets_for_Effective_Combination_Therapies_in_Tumors_with_Unmet_Medical_Need
Study
EGAS00001004775
-
ENU_NCI_H508_cetuximab_fixed_concentration_project
Study
EGAS00001001744
-
ENU_NCI_H508_Cetuximab_SecondRound
Study
EGAS00001001745
-
Drug-perturbation-based stratification of blood cancer
Study
EGAS00001001746
-
Poikiloderma_syndrome_RNAseq
Study
EGAS00001000250
-
Latency and interval therapy affect the evolution in metastatic colorectal cancer
Study
EGAS00001003646
-
Myeloproliferative_Disease_Whole_Genomes
Study
EGAS00001000290
-
Whole Exome Sequencing of High grade T1 non-muscle invasive bladder cancer
Study
EGAS00001004603
-
Healthspan and lifespan extension by fecal microbiota transplantation in progeroid mice
Study
EGAS00001003656
-
Androgen deprivation therapy promotes an inflammatory and obesity-like microenvironment in periprostatic fat
Study
EGAS00001003286
-
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Study
EGAS00001001788
-
Genomic Signatures Reveal DNA Damage Response Deficiency in Brain Metastases of Colorectal Cancer
Study
EGAS00001003659
-
16 Year Life History and Genomic Evolution of an ER+ HER2- Breast Cancer
Study
EGAS00001004624
-
Detection of ctDNA in Plasma of Patients with Clinically Localised Prostate Cancer is Associated with Rapid Disease Progression
Study
EGAS00001004636
-
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___WGS
Study
EGAS00001003682
-
Whole Exome Sequencing of 15 Tumor/Normal pairs of inflammatory hepatocellular adenomas
Study
EGAS00001003686
-
Psoriatic_arthritis_WGS
Study
EGAS00001002822
-
Targeted_gene_fusion_sequencing__Fus_seq__in_mesothelioma
Study
EGAS00001000390
-
Pancreatic Cancer Sequencing Initiative OICR
Study
EGAS00001000395
-
Integrative genomic analyses reveal androgen-driven somatic alteration landscape in early-onset prostate cancer
Study
EGAS00001000400
-
A novel TP53-KPNA3 translocation defines a de novo treatment-resistant clone in osteosarcoma
Study
EGAS00001001805
-
Placental_genomics
Study
EGAS00001003297
-
QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments
Study
EGAS00001001822
-
Breast_cancer_topographs
Study
EGAS00001003698
-
Renal_habitat_WXS
Study
EGAS00001003703
-
Bulk-RNA Sequencing of high-grade pancreatic and non-pancreatic Neuroendocrine Neoplasms
Study
EGAS00001004861
-
RNA-seq consisting of FASTQ paired-end reads from cancer samples
Study
EGAS00001003724
-
Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness
Study
EGAS00001003288
-
Cancer and germline exomes consisting of FASTQ paired-end reads from melanoma and lung cancer samples
Study
EGAS00001003723
-
Infant_Spindle_Tumour_Study
Study
EGAS00001002935
-
Integrative sequencing reveals alterations in untreated and castration resistant prostate cancer
Study
EGAS00001000526
-
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
-
Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Study
EGAS00001004648
-
DNA Methylation loss coupled with mitotic cell division promotes immune evasion of tumours with high mutation load
Study
EGAS00001003731
-
Subtype specific progression from DCIS to invasive breast cancer
Study
EGAS00001001866
-
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
-
Chromothripsis in human breast cancer (HIPO K26K/H017/A017)
Study
EGAS00001004662
-
Organoid_Derivation_Project___GRCh38___RNAseq
Study
EGAS00001004677
-
Circulating Tumor DNA Analysis Detects Minimal Residual Disease and Predicts Recurrence in Patients with Stage II Colon Cancer
Study
EGAS00001001839
-
Tissue and plasma RNA from esophageal cancer and precursor lesions
Study
EGAS00001004939
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
Genomics_of_acral_lentiginous_melanoma
Study
EGAS00001003740
-
Copy number and mutation profiling of Stage 1 epithelial ovarian cancer biopsies
Study
EGAS00001004961
-
Orphan_Tumour_Study_NB
Study
EGAS00001003445
-
HCA_Female_Reproductive_Adult_WSSS_RNA
Study
EGAS00001004727
-
whole-genome sequencing in 17 ESCC cases and whole-exome sequencing in 71 cases
Study
EGAS00001000709
-
Genetic subclone heterogeneity of tumor-initiating cells in human colorectal cancer
Study
EGAS00001001857
-
SPECTA__NGS_Screening_Program_for_Efficient_Clinical_Trial_Access
Study
EGAS00001000728
-
CAF-S3 subset in human breast and ovarian cancers
Study
EGAS00001003344
-
Gene expression profile of mesothelial-derived carcinoma-associated fibroblasts
Study
EGAS00001003747