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BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - RPMI_BG_T=24hrs, on genome GRCh38
Dataset
EGAD00001002441
-
BLUEPRINT release August 2016, Bisulfite-Seq for Acute Promyelocytic Leukemia - CTR, on genome GRCh38
Dataset
EGAD00001002407
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - RPMI_LPS_T=4hrs, on genome GRCh38
Dataset
EGAD00001002432
-
BLUEPRINT release January 2015, ChIP-Seq for erythroblast
Dataset
EGAD00001001194
-
BLUEPRINT release January 2015, ChIP-Seq for monocyte
Dataset
EGAD00001001197
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - RPMI_LPS_T=24hrs, on genome GRCh38
Dataset
EGAD00001002302
-
Emirati T2T Assembly
Study
EGAS50000001235
-
Cohort A RNA sequencing
Study
EGAS50000000950
-
Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
-
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
-
Federated discovery and sharing of genomic data using Beacons
Blog
federated-discovery-using-beacons
-
Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Dataset
EGAD00001003404
-
Affymetrix_Exon_Array
Dataset
EGAD00010000936
-
Illumina_1M_SNP_Array
Dataset
EGAD00010000939
-
CyclomicsSeq_Healthy_Flongle
Dataset
EGAD00001010150
-
Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Study
phs002205
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
Study
EGAS00001000545
-
Heritable pulmonary arterial hypertension in a large Iberian family
Study
EGAS00001003123
-
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Study
EGAS00001004326
-
GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
Study
phs001074
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangements
Study
EGAS50000001047
-
Personalized Treatment of Sezary Syndrome through a CTLA4:CD28 Fusion
Study
phs000773
-
Benchmark and validation of whole exome sequencing of a trio and singleton
Study
EGAS00001000852
-
TK-EP862 - Patient-derived xenograft model of Posterior Fossa A Ependymoma - WSG data
Dataset
EGAD00001010008
-
Single Patient BRAF Mutant Brain Tumor, Pre- and Post-dabrafenib WES.
Study
phs001629
-
Myeloproliferative_Neoplasms__MPN__Targeted_Gene_Screen
Study
EGAS00001000406
-
Unraveling the genetic basis of a collagen migration defect in patients with a combined platelet dysfunction and reduced bone density
Dataset
EGAD00001000109
-
Mosaic_Colorectal_Metastasis
Study
EGAS00001000613
-
Mechanism of Action of Vitamin E in NAFLD
Study
phs001930
-
HIV-phyloTSI: Subtype-independent estimation of time since HIV-1 infection for cross-sectional measures of population incidence using deep sequence data
Study
EGAS50000000895
-
Targeted sequencing of Burkitt lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001004649
-
Mutations in SPINK2 induce azoospermia
Study
EGAS00001002450
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Genomic Analysis of Diffuse Large B Cell Lymphoma
Study
phs003634
-
Hi-C NTERA-2
Dataset
EGAD00010001249
-
RAGE engagement by SARS-CoV-2 enables monocyte infection and underlies COVID-19 severity
Study
EGAS00001007529
-
RFX6-mediated dysregulation defines human β cell dysfunction in early type 2 diabetes
Study
EGAS00001006273
-
CyclomicsSeq_PREDICT_R10
Dataset
EGAD00001010153
-
TRAIP patients
Dataset
EGAD00001001633
-
Sequencing of rare human histiocytic tumour
Dataset
EGAD00001002184
-
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Study
phs000545
-
Low Density Genotyping from the Fragile Families and Child Wellbeing Study
Study
phs002417
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML
Study
EGAS00001006565
-
Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021)
Study
EGAS00001004282
-
Melanoma_C32_ENU_resistance_to_Combination_Therapy
Study
EGAS00001001614
-
Melanoma_C32_ENU_Resistance_to_Single_Agent_Therapy
Study
EGAS00001001697
-
Immune signature of malignant melanoma in pregnancy
Study
EGAS50000000492