-
RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser.
Study
EGAS00001007553
-
SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors
Study
EGAS00001007590
-
Genome-wide association study identifies common variants associated with breast cancer in South African Black women
Study
EGAS00001008032
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
-
Epigenetic, transcriptome and TF analysis of human NK cell and T cells
Dataset
EGAD00001008449
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Dataset
EGAD00001006151
-
CRUK-ICGC Prostate DNA Methylation Sequencing Dataset (Prostatectomy Batches 1-6)
Dataset
EGAD00001010184
-
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
-
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Dataset
EGAD00001006287
-
Longitudinal RNA-seq datasets from patients after abdominal surgery
Dataset
EGAD00001011102
-
Pre-clinical evolution of haematological malignancies_TGS
Dataset
EGAD00001006424
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Dataset
EGAD00001011363
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - scRNA
Dataset
EGAD00001011647
-
Using genetics to identify cell types and mechanisms underlying susceptibility to primary sclerosing cholangitis
Dataset
EGAD00001011815
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma RNA
Dataset
EGAD00001014788
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Dataset
EGAD00001015255
-
Genomic Advances in Sepsis (GAinS) genotyping
Dataset
EGAD00001015369
-
Exome sequencing of UK Birth Cohorts - Born in Bradford
Dataset
EGAD00001015370
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015378
-
Single-Cell Atlas of Common Variable Immunodeficiency shows germinal center-associated epigenetic dysregulation in B cell responses
Dataset
EGAD00001008575
-
PSCP_bisulphite analysis in hESCs
Dataset
EGAD00001002235
-
Cell of Origin and Early Evolution of Leukemia in Down Syndrome
Dataset
EGAD00001006555
-
Exome Sequencing of Spanish Patients with rare genetic diseases.
Dataset
EGAD00001005498