Study
Identification of Recurrent SMO and BRAF Mutations in Ameloblastomas
Study ID | Alternative Stable ID | Type |
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phs000739 | Cohort |
Study Description
RNA-seq data from two cases of ameloblastoma was analyzed for candidate gene fusions and point mutations. Recurrent point mutations identified in the RNA-seq data, as well as mutations identified with limited panel targeted deep sequencing, were validated as somatic. Expanding to a larger cohort of 28, one of two activating mutations was found in 80% of cases. No recurrent gene fusions events were identified.
Archive | Link Archive Accession |
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dbGaP | phs000739 |
Who archives the data?
