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bulk RNA-seq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000789
-
Idiopathic Collapsing Glomerulopathy in Brazilian patients
Study
EGAS50000000064
-
iPSC and iPSC derived pericytes
Dataset
EGAD50000000255
-
Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Study
EGAS00001007686
-
ScRNA-seq of human kidney immune cells of patients with ANCA-associated glomerulonephritis, Lupus Nephritis against a "healthy" nephrectomy control
Study
EGAS50000000159
-
Novel Gene-Environment Regulatory Circuit in Chamber-Specific Growth of Perinatal Heart
Study
phs002725
-
Chromothripsis orchestrates leukemic transformation in blast phase MPN through targetable amplification of DYRK1A
Study
EGAS00001007483
-
Discordant_Monozygotic_Twins_ALS(Genetics)
Study
EGAS50000000908
-
Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Study
EGAS00001002106
-
Genomic Landscape of Pediatric Myelodysplastic Syndromes
Study
EGAS00001002202
-
Emirati T2T Assembly
Study
EGAS50000001235
-
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
-
Cohort A RNA sequencing
Study
EGAS50000000950
-
Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
Federated discovery and sharing of genomic data using Beacons
Blog
federated-discovery-using-beacons
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RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Dataset
EGAD00001003404
-
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
-
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
-
Warm_autopsy__mutational_signatures_and_clonal_units
Study
EGAS00001002216
-
Mechanism of Action of Vitamin E in NAFLD
Study
phs001930
-
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
-
A Multi-Gene Mutation Classification of 468 Colorectal Cancers Reveals a Prognostic Role for APC
Study
phs001111
-
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
-
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
-
Clonal tracing with somatic epimutations reveals dynamics of blood aging
Study
EGAS00001008056
-
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
-
Angelman, Rett, Prader-Willi Syndromes Consortium (ARP) Angelman Syndrome Natural History Protocol
Study
phs000576
-
Mutations in GNAI2 Cause Developmental and Immune Dysregulation
Study
phs002817
-
Cas9-targeted-based long-read sequencing for genetic screening of RPE65 locus
Study
EGAS50000000596
-
An atlas of transcribed enhancers across helper T cell diversity for decoding human diseases
Study
JGAS000689
-
Rare Germline Variants in CDKN2A-Negative Children and Adolescents with Cutaneous Melanoma
Study
EGAS50000001311
-
Whole_Genome_Sequencing_of_JK_Family
Study
EGAS00001001323
-
miRNA_expression_in_response_to_LPS_stimulus_in_macrophages
Study
EGAS00001000691
-
Genomic study of an AT-AML
Study
EGAS00001004392