Data provider Accession Acronym URL
EGAO00000000108 CGP-UT

This data provider is associated with 9 studies:

Study Accessionsort descending Title
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.
EGAS00001000661 Whole-exome analysis of corticotropin-independent Cushing's syndrome
EGAS00001000875 Loss of functional mutation in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan Anemia
EGAS00001001103 Whole-exome sequencing of Fanconi anemia