-
Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
Study
EGAS00001000399
-
Whole genome sequencing and whole exome sequencing of mucosal melanoma
Study
EGAS00001000474
-
Whole genome sequencing of acral melanomas
Study
EGAS00001000486
-
POT1_splice_site_mutant_analysis
Study
EGAS00001000571
-
Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
Study
EGAS00001000510
-
Whole exome sequencing of peripheral T-cell lymphoma (PTCL)
Study
EGAS00001000557
-
WES cutaneous and uveal melanoma liver metastases
Study
EGAS00001004795
-
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
-
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Study
EGAS00001000643
-
Institut Curie Neuroblastoma data access Committee
Dac
EGAC00001000319
-
CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
-
FACS sorting of ploidy populations in an undifferentiated soft tissue sarcoma for RRBS
Study
EGAS00001006143
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
Validation of a targeted sequencing panel for multiple myeloma
Study
EGAS00001006164
-
Small molecule inhibitors of LOXL synergize with 5-AZA to restore erythropoiesis in myeloid neoplasms
Study
EGAS00001006174
-
Study of pediatric hepatocellular carcinoma caused by bile salt export pump deficiency
Study
EGAS00001000749
-
Primary Neuroblastoma Circle-seq
Study
EGAS00001004797
-
Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Study
EGAS00001000750
-
Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
-
Integrated genetic and epigenetic analysis defines novel molecular clusters in rhabdomyosarcoma
Study
EGAS00001000884