-
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
-
Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers
Study
EGAS00001002604
-
Whole exome sequencing of 76 individuals with familial atrial fibrillation
Study
EGAS00001003207
-
FBSeq: RNA sequencing of human fetal brain.
Study
EGAS00001003214
-
Genomic landscape of oral cancers (Illumina WGS)
Study
EGAS00001003228
-
An exome sequencing approach to defining the genetic risk factors for Achilles tendinopathy
Study
EGAS00001003234
-
A mechanistic classification of clinical phenotypes in neuroblastoma
Study
EGAS00001003244
-
46 CLL Whole Genome Sequencing Study
Study
EGAS00001003254
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Study
EGAS00001003367
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
Embryonic tumour transmission in monozygotic twins
Dataset
EGAD00001015681
-
Duplexseq of the interstrand crosslinks_WGS
Dataset
EGAD00001010298
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - RNA-Seq
Dataset
EGAD00001009794
-
Exome Atlas in HCC tumors
Dataset
EGAD00001015342
-
Exome Sequencing of 44 subjects with very severe or fatal COVID-19
Dataset
EGAD00001008993
-
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Dataset
EGAD00001009668
-
Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Dataset
EGAD00001009647
-
Anthropological dataset 1 for The admixture histories of Cabo Verde
Dataset
EGAD00001008976
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - WGS
Dataset
EGAD00001009793
-
Diagnostic utility of whole genome sequencing in adults with B-other acute lymphoblastic leukemia
Dataset
EGAD00001009304
-
Diagnostic utility of whole genome sequencing in adults with B-other acute lymphoblastic leukemia - RNA
Dataset
EGAD00001009305
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Dataset
EGAD00001009847
-
Population-based analysis of POT1 variants in a cutaneous melanoma case-control cohort
Dataset
EGAD00001009848
-
Somatic mutation and clonal evolution normal breast tissue WGS
Dataset
EGAD00001010123
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (tumour data)
Dataset
EGAD00001010274
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - WGS
Dataset
EGAD00001010872
-
Anthropological dataset 2 for The admixture histories of Cabo Verde
Dataset
EGAD00001008977
-
Clonal origin of lineage switch leukemia following CAR-T cell and blinatumomab therapy
Dataset
EGAD00001009161
-
Oropharyngeal Squamous Cell Carcinoma Mutanome
Dataset
EGAD00001009167
-
Linguistic utterance counts for The admixture histories of Cabo Verde
Dataset
EGAD00001008978
-
Epigenomic analysis of human dopaminergic neuron differentiation reveals LBX1, NHLH1 and NR2F1/2 as necessary for lineage specification
Dataset
EGAD00001009288
-
Single-cell study of 14 childhood medulloblastoma patients
Dataset
EGAD00001009057
-
Convergent somatic evolution from early life in a germline ribosomopathy
Dataset
EGAD00001009061
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - WGS
Dataset
EGAD00001011645
-
RNAseq data
Dataset
EGAD00001009728
-
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Dataset
EGAD00001009280
-
HELIUS cohort gut microbiome batch2
Dataset
EGAD00001009732
-
Tracking the evolution of esophageal squamous cell carcinoma under dynamic immune selection by multi-omics sequencing
Dataset
EGAD00001009482
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
Human Origins array data for 1510 individuals
Dataset
EGAD00001010015
-
Genomic Analysis of a Metastatic Fusion-negative Embryonal Rhabdomyosarcoma
Dataset
EGAD00001009973
-
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Dataset
EGAD00001010103
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (normal data)
Dataset
EGAD00001010295
-
CRUK-ICGC Prostate DNA Methylation Sequencing Dataset (Prostatectomy Batches 1-6)
Dataset
EGAD00001010184
-
Raw data for "Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse"
Dataset
EGAD00001010260
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - TGS
Dataset
EGAD00001010874
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010913
-
Somatic L1 retrotransposition in normal colorectal epthelium
Dataset
EGAD00001010183
-
Influence of the Microbiome on Epigenetic Mechanisms in IBD
Dataset
EGAD00001011066
-
Longitudinal RNA-seq datasets from patients after abdominal surgery
Dataset
EGAD00001011102
-
Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
-
Capture-based NGS
Dataset
EGAD00001011151
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Dataset
EGAD00001011260
-
Genetic determinants of monocyte splicing are enriched for disease susceptibility loci including for COVID-19
Dataset
EGAD00001010176
-
Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Dataset
EGAD00001011340
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Dataset
EGAD00001011067
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Dataset
EGAD00001011363
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma RNA
Dataset
EGAD00001014788
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma RNA
Dataset
EGAD00001014790
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Dataset
EGAD00001015255
-
Exome sequencing of UK Birth Cohorts - Born in Bradford
Dataset
EGAD00001015370
-
Exome sequencing of UK Birth Cohorts - Millennium Cohort Study
Dataset
EGAD00001015372
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - scRNA
Dataset
EGAD00001011647
-
Genetic regulation of RNA splicing in human pancreatic islets
Dataset
EGAD00001009102
-
Genotype data for The admixture histories of Cabo Verde - genotype data
Dataset
EGAD00001008979
-
Single cell transcriptional evolution of myeloid leukaemia of Down syndrome – scRNA
Dataset
EGAD00001015452
-
HSP90 inhibitor resistant K562 cells
Dataset
EGAD00001009051
-
Genomic Advances in Sepsis (GAinS) genotyping
Dataset
EGAD00001015369
-
DERMATLAS: Hidradenoma papilliferum_WES
Dataset
EGAD00001015481
-
A spatiotemporal cancer cell trajectory underlies glioblastoma heterogeneity
Dataset
EGAD00001015516
-
Single-cell omics data for COVID-19 patients
Dataset
EGAD00001009331
-
PacBio Rare Disease Study
Dataset
EGAD00001015611
-
Cancers of Unknow Primary
Dataset
EGAD00001009426
-
RNAseq dataset for MALT1 in MCL
Dataset
EGAD00001009771
-
Whole-Genome Sequences from five human populations of Sudan
Dataset
EGAD00001015636
-
Selection of somatic escape variants in SERPINA1 in liver tissue of patients with alpha-1 anti-trypsin deficiency - WGS
Dataset
EGAD00001015430
-
Genetic landscape of Extranodal NK/T-cell lymphoma
Dataset
EGAD00001009852
-
Understanding the development of resident memory T cells (Trm) in the human small intestine using integrative multiomic approaches: Adult RNA (2025-10-14)
Dataset
EGAD00001015739
-
Ancestry and somatic profile predict acral melanoma origin and prognosis – WXS
Dataset
EGAD00001015755
-
A next-generation dual guide CRISPR system for genetic interaction library screening
Dataset
EGAD00001015754
-
Ancestry and somatic profile predict acral melanoma origin and prognosis – RNA
Dataset
EGAD00001015756
-
Using genetics to identify cell types and mechanisms underlying susceptibility to primary sclerosing cholangitis
Dataset
EGAD00001011815
-
Comprehensive Deep Sequencing Atlas in HCC tumors
Dataset
EGAD00001015343
-
Genetic architecture of male infertility in India
Dataset
EGAD00001015606
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015378
-
Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015477
-
DERMATLAS: Hidradenoma papilliferum_RNAseq
Dataset
EGAD00001015480
-
Mapping Cells and Interactions in the Thymus Across Development and Aging (2025-07-28)
Dataset
EGAD00001015660
-
DNMT3A-R882 mutations intrinsically drive dysfunctional neutropoiesis from human haematopoietic stem cells
Dataset
EGAD00001015750
-
Single cell transcriptional evolution of myeloid leukaemia of Down syndrome – WGS
Dataset
EGAD00001015453
-
Timing the Philadelphia chromosome and trajectory to chronic myeloid leukaemia
Dataset
EGAD00001015353
-
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Dataset
EGAD00001015357
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015376
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015377
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma WES
Dataset
EGAD00001014787
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010914
-
Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer
Dataset
EGAD00001011297
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - RNA
Dataset
EGAD00001011646