-
Large scale familial CRC exome sequencing study
Study
EGAS00001001666
-
Comparison of HCC cell lines and primary HCCs
Study
EGAS00001001678
-
Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
-
TCR β-chain repertoire characterization of regulatory and conventional T cells in breast tumors from breast cancer patients.
Study
EGAS00001004671
-
Accurate mutation detection in leukemia by re-sequencing a cancer gene set
Study
EGAS00001000268
-
Automated system for scoring hematoxylin and eosin-stained ovarian cancer sections by identifying single cells uncovered that stromal cell ratio is a significant predictor for overall survival and progression-free survival.
Study
EGAS00001001694
-
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency
Study
EGAS00001002200
-
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
-
Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer
Study
EGAS00001005981
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-4)
Study
EGAS00001006101
-
Exome sequencing of paired primary tumor and metastatic breast cancer
Study
EGAS00001004578
-
Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing)
Study
EGAS00001002784
-
PanProstate Cancer Group UK data
Study
EGAS00001002876
-
Discovery of new fusion transcripts in a cohort of pediatric solid cancers at relapse
Study
EGAS00001003236
-
Genetic alterations in metastatic uveal melanoma
Study
EGAS00001003303
-
Korean Young Age Diffuse Gastric Cancers
Study
EGAS00001001711
-
Genome-wide DNA methylation profiles of NSCLC xenograft and primary lung tissues for the identification of epigenetic predictive biomarkers.
Study
EGAS00001002479
-
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
Korean Gastric cancers data
Dac
EGAC00001000439
-
CRC GWAS on the Spanish population
Study
EGAS00001003633
-
A PROSTATE TUMORGRAFT PANEL TO ACCELERATE PRECISION MEDICINE
Study
EGAS00001007033
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
-
GBM cancer stem cell lines -RNA-seq and WGS data
Study
EGAS00001003700
-
Ulcerative colitis study - WES data
Study
EGAS00001003801
-
Preservation of stemness in high-grade serous ovarian cancer organoids requires low Wnt environment
Study
EGAS00001003821
-
The evolutionary steps from primary to metastatic prostate cancer are largely uncharted, and the ability to use DNA present in body fluids as correlates of aggregate metastatic status is under-examined. We reconstructed phylogenies in ten prostate cancer patients with fatal disease using deep targeted sequencing of the prostate, adjacent and distant organs, as well as plasma, serum, and cerebrospinal fluid at various time points. A total of 163 samples are studied.
Study
EGAS00001003848
-
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
-
Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Study
EGAS00001003928
-
genome-wide cfDNA methylation analysis
Study
EGAS00001003958
-
SCLC tumor sequencing
Study
EGAS00001003985
-
SCLC ctDNA sequencing
Study
EGAS00001003984
-
High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune contexture, clinical outcome and sensitivity to targeted therapies
Study
EGAS00001004612
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 1).
Study
EGAS00001002630
-
White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer
Study
EGAS00001004114
-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
Inferring expressed genes by whole-genome sequencing of plasma DNA
Study
EGAS00001001754
-
Single Cell RNAseq of blood and tumor from renal cancer patients
Study
EGAS00001004230
-
Whole exome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004231
-
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Study
EGAS00001004064
-
Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Study
EGAS00001005549
-
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Study
EGAS00001002646
-
TP53 variant detection analysis in high grade serous epithelial ovarian cancer
Study
EGAS00001004361
-
Subtype specific studies of breast cancer progression. Milan cohort.
Study
EGAS00001004390
-
Comparing nodal versus bony metastatic spread using tumour phylogenies
Study
EGAS00001001801
-
Mutational_burden_in_human_hair_follicles
Study
EGAS00001004462
-
Immunoreactive_p53_areas_in_human_skin_2
Study
EGAS00001004463
-
RNA sequencing data of 66 matched primary and recurrent high grade serous ovarian cancer
Study
EGAS00001002660
-
A novel TP53-KPNA3 translocation defines a de novo treatment-resistant clone in osteosarcoma
Study
EGAS00001001805
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
Resident memory CD8 T cell in human lung cancer
Study
EGAS00001004707
-
WGS of 32 paired SRCC samples
Study
EGAS00001002668
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments
Study
EGAS00001001822
-
Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma
Study
EGAS00001004753
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
-
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
-
CancerLocator: Non-Invasive Cancer Diagnosis and Tissue-of-Origin Prediction Using Methylation Profiles of Cell-Free DNA
Study
EGAS00001002211
-
Tumor HTG EdgeSeq from metastatic castrate resistant prostate cancer
Study
EGAS00001004852
-
Sequencing of liver cancer cell lines
Study
EGAS00001002237
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
EAC Genomic data
Study
EGAS00001004887
-
Circulating Tumor DNA Analysis Detects Minimal Residual Disease and Predicts Recurrence in Patients with Stage II Colon Cancer
Study
EGAS00001001839
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Study
EGAS00001004975
-
Longitudinal single-cell RNA-seq data of metastatic ovarian cancer
Study
EGAS00001005006
-
RNA sequencing of PTCL-NOS
Study
EGAS00001005015
-
Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data
Study
EGAS00001000659
-
Stromal cell diversity associated with immune evasion in human triple‐negative breast cancer
Study
EGAS00001005061
-
Subtype specific progression from DCIS to invasive breast cancer
Study
EGAS00001001866
-
Targeted next-generation sequencing of 13 chordoid gliomas of the third ventricle
Study
EGAS00001002733
-
early-Duodenal Cancer sequencing study
Study
EGAS00001006357
-
H021-Master Umbrella study2 (not to be released)
Study
EGAS00001005145
-
Multi-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors
Study
EGAS00001001871
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Study
EGAS00001005182
-
Analysis of Multiparametric MR imaging and tumor tissue sampling to identify response and acquired resistance to HIF-2 inhibition in patients with advanced clear cell renal cell carcinoma enrolled in a phase 1, multiple-dose, dose-escalation trial of PT2385, a HIF-2alpha inhibitor
Study
EGAS00001003506
-
Genomic and Transcriptomic Profile of Paired Primary-Metastasis Colorectal Tumors
Study
EGAS00001005276
-
ChIP-seq in colorectal cancer and paired adjacent normal mucosa
Study
EGAS00001005303
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
-
Evolutionary analysis of primary tumors and metastatic lesions from 20 breast cancer patients (99 samples in total) using exome sequencing data.
Study
EGAS00001002737
-
NOWAC blood-based breast cancer case-control study
Study
EGAS00000000134
-
Identification_and_functional_validation_of_driver_mutations_in_colorectal_cancer
Study
EGAS00001000044
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Whole Exome Sequencing of Localized Prostate Cancer Patients
Study
EGAS00001005685
-
Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing
Study
EGAS00001000370
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
DNA methylation and Panel sequencing for pancreatic neuroendocrine carcinomas (PanNECs) and pancreatic neuroendocrine tumors (PanNETs)
Study
EGAS00001005731
-
Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency
Study
EGAS00001000149
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
The genomic landscape of large and small tumors in early-onset prostate cancer patients
Study
EGAS00001000383
-
Exome Sequencing of Gastric Cancer
Study
EGAS00001000153
-
Complete Genomics paired end sequencing; Ovarian cancer
Study
EGAS00001000158
-
Whole genome sequencing of matched primary and metastatic acral melanomas
Study
EGAS00001000169
-
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Study
EGAS00001005827
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer Genes in Endometrial Cancer
Study
EGAS00001000318