EGAO00000000048

Data provider Accession Acronym URL
EGAO00000000048 Not Provided

This data provider is associated with 13 studies:

Study Accessionsort descending Title
EGAS00000000105 Copy number analysis of Diamond-Blackfan Anemia (DBA) using SNP array
EGAS00001000275 AML targeted resequencing study
EGAS00001000371 Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia
EGAS00001000509 an integrated molecular study of clear cell renal cell carcinoma (ccRCC) including whole-genome/exome and RNA sequencing as well as array-based gene expression/copy-number/methylation analyses
EGAS00001000521 Whole exome and whole genome sequencing of juvenile myelomonocytic leukemia (JMML)
EGAS00001000546 Landscape of gene mutations in Down syndrome-related myeloid disorders
EGAS00001000557 Whole exome sequencing of peripheral T-cell lymphoma (PTCL)
EGAS00001000646 The study provides comprehensive access to the set of EGA studies which may be useful as controls.
EGAS00001000958 TGS Comprehensive Molecular Characterization of Colorectal Cancer Metastases MOSAIC
EGAS00001001054 GIST SSGXVIII trial targeted gene sequencing
EGAS00001001095 NGS based viability screening using haploid cell line
EGAS00001001145 FWO project G 0687 12 X10 WGS
EGAS00001001155 Anaplastic Meningioma V3 cancer gene panel