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Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Study
EGAS00001002874
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Whole genome sequencing delineates regulatory, structural, and cryptic splice variants in early onset cardiomyopathy
Study
EGAS00001004929
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Epigenetic and transcriptional profile of memory B cells in Multiple sclerosis
Study
EGAS50000000872
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Comprehensive biomarker analysis from phase II study of nivolumab in patients with thymic carcinoma
Study
JGAS000588
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Expression profiling of Gorlin iPSCs in the osteoblast induction culture
Study
JGAS000218
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Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
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Effect of the Placental Transcriptome on Stunting in a Longitudinal African Cohort
Study
phs001782
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shallow Whole-Genome sequencing of 14 TNBC tumor in the MATADOR trial - for in silico spike-in experiment
Dataset
EGAD50000001863
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DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001108
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DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001060
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Multi-omics analyses of airway host-microbe interactions in chronic obstructive pulmonary disease identify potential therapeutic interventions
Study
EGAS00001006398
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Genetic Analysis of Tuberous Sclerosis Complex (TSC) Hypomelanotic Macules
Study
phs001236
-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
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Altered oligodendrocyte heterogeneity in Multiple sclerosis revealed by single nuclei RNA sequencing
Study
EGAS00001003412
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CASCADE metastatic melanoma study
Study
EGAS00001004950
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Base-excision repair pathway shapes 5-methylcytosine deamination signatures in pan-cancer genomes
Study
EGAS50000000536
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Role of Microglia Somatic Mutations in Neurodegenerative Diseases
Study
phs002213
-
A single-chain derivative of the integrin β1-activating TS2/16 antibody potentiates organoid growth in Matrigel and Collagen hydrogels.
Study
EGAS50000001113
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Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
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Whole-genome plasma sequencing reveals focal amplifications as a driving force in metastatic prostate cancer
Study
EGAS00001001018
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Rare occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers
Study
EGAS00001005909
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The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Study
EGAS00001005935
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Disease specific alterations in the olfactory mucosa of patients with Alzheimer’s disease
Study
EGAS00001006019
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The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Study
EGAS00001001515
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Somatic mutations predict an aggressive phenotype in meningioma but do not drive grade progression
Study
EGAS00001006585