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Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Study
EGAS00001003430
-
Dedifferentiated_Melanoma
Study
EGAS00001003471
-
Molecular phenotyping of MCA/ID patients to improve diagnosis
Study
EGAS00001003489
-
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Study
EGAS00001003536
-
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
-
Dedifferentiated_Melanoma_RNAseq
Study
EGAS00001003601
-
Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia
Study
EGAS00001003627
-
Oral mucosa organoids as a potential model for personalized therapies
Study
EGAS00001003628
-
Mapping_genetic_variants_underlying_gene_regulation_in_healthy_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Study
EGAS00001003647
-
Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Study
EGAS00001003746
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003136
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003138
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_TGS
Study
EGAS00001002858
-
Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES
Study
EGAS00001002863
-
Somatic_mutation_and_clonal_evolution_normal_breast_tissue_WGS
Study
EGAS00001002857
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Study
EGAS00001003502
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___Exome__Novaseq_
Study
EGAS00001003527
-
Renal_habitat_WXS
Study
EGAS00001003703
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period.
Study
EGAS00001002955
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Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195