-
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
-
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
-
Single nucleus and in situ RNA sequencing reveals cell topographies in the human pancreas
Study
EGAS00001004653
-
Tissue and plasma RNA from esophageal cancer and precursor lesions
Study
EGAS00001004939
-
RNA-seq from human embryonic tissues (additional samples 2018)
Study
EGAS00001003738
-
whole-genome sequencing in 17 ESCC cases and whole-exome sequencing in 71 cases
Study
EGAS00001000709
-
Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin
Study
EGAS00001001875
-
Hi-C dataset for testicular germ cell tumour GWAS risk loci, as described in the Oncoarray Litchfield et al. 2016 paper.
Study
EGAS00001001930
-
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
-
Physiological and genetic adaptations to diving in Sea Nomads
Study
EGAS00001002823
-
Immune trajectory of response and adverse effect in immunotherapy-treated hepatocellular carcinoma
Study
EGAS00001004843
-
The Acquisition of Molecular Drivers in Pediatric Therapy-Related Myeloid Neoplasms
Study
EGAS00001004850
-
Single_Cell_RNAseq_at_various_stages_of_HiPSCs_differentiating_toward_definitive_endoderm_and_endoderm_derived_lineages
Study
EGAS00001002278
-
UK renal cancer samples genotyped on Illumina OmniExpress BeadChip
Study
EGAS00001002336
-
Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity
Study
EGAS00001005227
-
Longitudinal Single-Cell Profiling Reveals Molecular Heterogeneity and Tumor-Immune Evolution in Refractory Mantle Cell Lymphoma
Study
EGAS00001005019
-
HSC_colony_many_years_post_allogeneic_bone_marrow_transplant_TGS
Study
EGAS00001005298
-
Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma
Study
EGAS00001005314
-
Real-time response profiling through serial plasma analyses during FOLFOX treatment in patients with colorectal cancer
Study
EGAS00001004213
-
Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer
Study
EGAS00001005108
-
Genomic landscape and PD-1 blockade in Natural-killer/T cell lymphoma
Study
EGAS00001003828
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325
-
Molecular profiling of metastatic uveal melanoma
Study
EGAS00001004296
-
Single_cell_analysis_of_cytokine_induced_T_cell_states
Study
EGAS00001003215
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
Molecular evolution and clinical trajectories of prostate cancer identifies novel markers for risk stratification
Study
EGAS00001002923
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Study
EGAS00001002936
-
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas
Study
EGAS00001004461
-
A Single-Cell Atlas of the Multicellular Ecosystem of Primary and Metastatic Hepatocellular Carcinoma
Study
EGAS00001004468
-
COVID19 Host Genetic Initiative
Study
EGAS00001005304
-
Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer
Study
EGAS00001003892
-
Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Study
EGAS00001002953
-
Sequence data for study: Mobilization of tissue-resident memory CD4+ T lymphocytes from bone marrow and their contribution to a systemic secondary immune reaction
Study
EGAS00001005475
-
Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
-
Interethnic comparability in blood pressure GWAS
Study
EGAS00001002991
-
Familial adult myoclonic epilepsy in Sri Lankan and Indian families
Study
EGAS00001004012
-
Mutations in the RAS/MAPK pathway drive replication repair deficient hypermutated tumors and confer sensitivity to MEK inhibition
Study
EGAS00001005008
-
scRNA-seq of LN and lymphoma stroma
Study
EGAS00001005732
-
Using de novo assembly to identify structural variation of complex immune system gene regions
Study
EGAS00001005046
-
Immune profiling reveals enrichment of distinct immune signatures in high-risk oral potentially malignant disorders
Study
EGAS00001005520
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
CRISPR transduction of iPS cells
Study
EGAS00001005102
-
The genomic landscape of early stage ovarian high grade serous carcinoma
Study
EGAS00001005567
-
A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158
-
Integrative molecular analysis of pediatric Anaplastic large cell lymphoma reveals subtypes with distinct immune suppression signatures.
Study
EGAS00001004189
-
Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes
Study
EGAS00001004235
-
A microRNA-signature that correlates with cognition and is a target against cognitive decline
Study
EGAS00001005627
-
Single-cell RNA-seq of bronchoalveolar lavage (BAL) fluid of late stage severe COVID-19 patients
Study
EGAS00001005634
-
Genetic and immune landscape evolution defines subtypes of MMR deficient colorectal cancer
Study
EGAS00001005769
-
Rare occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers
Study
EGAS00001005909
-
Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort
Study
EGAS00001005900
-
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set)
Study
EGAS00001004314
-
A molecular signature for IL-10-producing Th1 cells in protozoan parasitic diseases
Study
EGAS00001004454
-
Combined clinical and gene expression score identifies high-risk individuals among follicular lymphoma patients on immunotherapy
Study
EGAS00001002566
-
The evolution of hematopoietic cells under cancer therapy
Study
EGAS00001005234
-
Fibroblast heterogeneity drives metastatic spread in breast cancer through distinct mechanisms
Study
EGAS00001003238
-
Myoepithelial progenitors as founder cells of hyperplastic human breast lesions upon PIK3CA transformation
Study
EGAS00001005933
-
Ductal keratin 15+ luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
Study
EGAS00001005963
-
The genomic and immune landscape of long-term survivors of high-grade serous ovarian cancer
Study
EGAS00001005984
-
Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Study
EGAS00001003232
-
Homologous recombination DNA repair deficiency and PARP inhibition activity in primary triple negative breast cancer
Study
EGAS00001004405
-
Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring
Study
EGAS00001004406
-
SARS‐CoV‐2 receptor ACE2 and TMPRSS2 are primarily expressed in bronchial transient secretory cells
Study
EGAS00001004419
-
Methylome sequencing of cell-free DNA and RRBS of solid tissue
Study
EGAS00001006020
-
Somatic_mutation_profiling_of_intestinal_crypts_from_IBD_Full_STDY
Study
EGAS00001003249
-
Custom long non-coding RNA capture enhances detection sensitivity in different human sample types.
Study
EGAS00001005418
-
Detection of cell-free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients
Study
EGAS00001003255
-
CCL22 chemokine mutations drive natural killer cell lymphoproliferative disease by biasing GPCR signaling
Study
EGAS00001006009
-
ENCORAFENIB COMBINED WITH BINIMETINIB FOR BRAFV600E-MUTATED RELAPSED/REFRACTORY MULTIPLE MYELOMA: THE PHASE II GMMG-BIRMA TRIAL (Hipo_K08K)
Study
EGAS00001005973
-
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Study
EGAS00001005982
-
Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab
Study
EGAS00001006004
-
A Proteogenomic Analysis of Clear Cell Renal Cell Carcinoma in a Chinese Population
Study
EGAS00001006005
-
HSC_colony_many_years_post_allogeneic_bone_marrow_transplant___Bait_set_2
Study
EGAS00001005534
-
Oncogenic cooperation in a human de novo T-ALL model
Study
EGAS00001006055
-
Molecular and functional profiling of plasmablastic lymphoma
Study
EGAS00001004659
-
Enhanced cortical neural stem cell identity through SMAD/WNT inhibition in human cerebral organoids facilitates emergence of outer radial glial cells
Study
EGAS00001006063
-
single cell RNA-seq and ATAC-seq of human fetal forebrain tissue
Study
EGAS00001006136
-
A comprehensive characterization of the cell-free transcriptome reveals tissue- and subtype-specific biomarkers for cancer detection
Study
EGAS00001004704
-
Whole genome sequencing of EBV Associated Nasopharyngeal Carcinoma
Study
EGAS00001004705
-
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements
Study
EGAS00001003415
-
Comprehensive genomic and transcriptomic analysis of three synchronous primary tumours and a recurrence from a head and neck cancer patient
Study
EGAS00001004857
-
Genomic analysis of a hypermutated gliosarcoma
Study
EGAS00001004864
-
The effect of pre-analytical and physiological variables on cell-free DNA fragmentation
Study
EGAS00001005748
-
The immunopeptidome landscape associated with T cell infiltration, inflammation and immune-editing in lung cancer
Study
EGAS00001006298
-
Exome sequencing of synchronous colorectal cancers
Study
EGAS00001003474
-
The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Study
EGAS00001005935
-
RNA-seq on patient-derived, stage II, CRC cell lines
Study
EGAS00001005948
-
The Proteogenomic Subtypes of Acute Myeloid Leukemia
Study
EGAS00001005950
-
Combined gene expression and digital pathology identifies molecular mediators of T cell exclusion and immune suppression in ovarian cancer
Study
EGAS00001003487
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006233
-
Human genome-wide variations in the Massim region
Study
EGAS00001006010
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
Phase 1 CX-5461 Trial (Canadian Cancer Trials Group Trial IND.231)
Study
EGAS00001006173
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities
Study
EGAS00001006422
-
MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__Exome__Novaseq_
Study
EGAS00001003528
-
Arriba: accurate and efficient detection of gene fusions from RNA-Seq (H021)
Study
EGAS00001003554