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Whole Genome Sequencing of Neuroblastoma
Study
EGAS00001000222
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Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
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Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
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Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
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Whole genome sequencing and whole exome sequencing of mucosal melanoma
Study
EGAS00001000474
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Whole genome sequencing of acral melanomas
Study
EGAS00001000486
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POT1_splice_site_mutant_analysis
Study
EGAS00001000571
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Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
Study
EGAS00001000510
-
Whole exome sequencing of peripheral T-cell lymphoma (PTCL)
Study
EGAS00001000557
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WES cutaneous and uveal melanoma liver metastases
Study
EGAS00001004795
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Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
Whole genome sequencing of metastatic melanomas from a patient with primary resistance to BRAF inhibition
Study
EGAS00001000580
-
Neuroblastoma Cell Line Circle-seq
Study
EGAS00001004796
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
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Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Study
EGAS00001000643
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Institut Curie Neuroblastoma data access Committee
Dac
EGAC00001000319
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CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653