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WGS___Mutant_clone_mapping_in_normal_oesohagus_and_skin
Study
EGAS00001002416
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Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
THAP11 mutations in a patient with a cblX-like phenotype implicates THAP11 in the regulation of cobalamin metabolism and early vertebrate development
Study
EGAS00001002201
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Profiling the unique protective properties of intracranial arterial endothelial cells
Study
EGAS00001004479
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma
Study
EGAS00001004564
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM066-WES
Study
EGAS00001004567
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM67 WES
Study
EGAS00001004555
-
Peripheral Blood Transcriptome Analysis of ALS Patients
Study
phs002055
-
Stromal-induced epithelial-mesenchymal transition induces drug resistance in acute lymphoblastic leukemia
Study
EGAS00001006120
-
P647 Targeted resequencing project
Dataset
EGAD00001000383