-
Combined single-cell transcriptomics and T-cell receptor sequencing reveal heterogeneity of mycosis fungoides between and within patients and identify a CD4+ cytotoxic subtype
Study
EGAS50000000226
-
DAC for Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Dac
EGAC50000000332
-
Transcriptome analysis of human longitudinal whole blood samples from PCR-positive and PCR-negative adults following controlled inoculation with Influenza A (H3N2) virus.
Study
EGAS50000000679
-
AYA glioma NGS
Study
EGAS50000000383
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Mapping Genotypes to Chromatin Accessibility Profiles in Single Cells
Study
EGAS50000000164
-
Fragmentomic features of individuals with different cfDNA concentrations
Study
EGAS50000000692
-
RNAseq samples of patients with anti-PD-1 resistant HNSCC from a non-randomized, open-label phase 1b clinical trial
Study
EGAS50000000728
-
WES samples of patients with anti-PD-1 resistant HNSCC from a non-randomized, open-label phase 1b clinical trial
Study
EGAS50000000729
-
Synchronous patterning of hiPSC-derived CNS progenitors generates comprehensive axial spinal cord organoids (CASCOs) containing diverse motor neuron population
Study
EGAS50000000891
-
Gliomas, glioneuronal and neuronal tumors
Dataset
EGAD50000000300
-
Ultrasensitive Detection and Monitoring of Circulating Tumor DNA using Structural Variants in Early-Stage Breast Cancer
Study
EGAS50000000799
-
Genome-wide NanoRCS sequencing of cfDNA and ctDNA from liquid biopsies of healthy individuals and cancer patients
Study
EGAS50000000154
-
Multi-omics profiling identifies two epithelioid sarcoma molecular subtypes with distinct signaling and immune characteristics
Dac
EGAC50000000552
-
Clinical Outcomes of 344 Diffuse Large B-Cell Lymphoma patients
Study
EGAS50000001054
-
DAC for Genomic landscapes of endometrioid and mucinous ovarian cancers and morphologically similar tumor types
Dac
EGAC50000000341
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
The acute effects of morning bright light on the human white adipose tissue transcriptome: exploratory post hoc analysis
Study
EGAS50000001206
-
Longitudinal analysis of bone marrow heterogeneity reveals the co-evolution of malignant B cells and their T-cell niche supporting follicular lymphoma persistence
Study
EGAS50000001295
-
RNA sequencing data from patient derived colorectal cancer organoids
Study
EGAS50000000685
-
DCIS Whole Exome & Whole Genome Sequencing Data
Dataset
EGAD50000001846
-
Single cell RNAseq data of human neurons, Bouwen et al Nat Comm 2025
Study
EGAS50000001369
-
Profiling the genomic landscape and evolutionary history of polyploid giant cancer cells in undifferentiated pleomorphic sarcomas
Study
EGAS50000001445
-
Investigating the differences in iPSC-derived intestinal epithelial cell behaviour and composition grown as organoid, in Transwell or Intestine-Chip.
Study
EGAS50000001339
-
A human induced pluripotent stem cell toolbox for studying sex chromosome effects-Whole exome seq
Study
EGAS50000000930
-
Single cell transcriptome and TCR sequencing of EBNA1, ANO2 and CRYAB-reactive T cells in multiple sclerosis.
Study
EGAS50000001531
-
Single cell transcriptomics to characterize the tumor microenvironment of prostate cancer fusion biopsies
Study
EGAS50000000888
-
Characterization of the cellular microenvironment in fibrostenotic Crohn’s disease
Study
EGAS50000000382
-
Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis
Study
EGAS50000000591
-
Spatial map of microglia states across CNS diseases
Study
EGAS50000001289
-
Multiplexed biomarkers dynamically detect heterogeneous residual neuroblastoma cell clone activity in the bone marrow niche
Study
EGAS50000001581
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00001000245
-
ICGC PanCancer Analysis of Whole Genomes
Study
EGAS00001001692
-
Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Study
EGAS00000000115
-
Deciphering the genomic, epigenomic and transcriptomic landscapes of pre-invasive lung cancer lesions to determine prognosis
Dataset
EGAD00001003883
-
Whole transcriptome RNA sequencing on bone marrow and peripheral blood samples from patients with acute myeloid leukemia at diagnosis or relapse.
Dataset
EGAD00001004187
-
Spatial heterogeneity of follicular lymphoma
Dataset
EGAD00001003553
-
GCT WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003267
-
CCOC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003265
-
Identification of cardiovascular biomarkers through an integrative omics approach
Dataset
EGAD00001002197
-
GoNL aligned sequence data in BAM format.
Dataset
EGAD00001001038
-
RNAseq data of polyA+ RNA from Leukocytes from 624 individuals of the SardiNIA cohort.
Study
EGAS00001002105
-
Assessment of de novo copy number variations in Italian patients with schizophrenia.
Study
EGAS00001002159
-
The aim of this project is to identify, on 15 French Caucasian and 10 African-Caribbean men, through an integrative approach of DNA sequencing and transciptomic analyses, relevant genomic events that characterize or allow targeting the various phenotypes of aggressiveness of early stages of prostate cancer.
Study
EGAS00001002176
-
Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Study
EGAS00001002495
-
Prostate Cancer and Normal Adjacent Prostate RNA-seq samples, NGS-ProToCol
Study
EGAS00001002816