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Measuring A-to-I RNA editing signatures of neuronal populations within the Drosophila brain

ABSTRACT: We used an improved INTACT (Isolation of Nuclei Tagged in A specific Cell Type) technique to isolate RNA from purified nuclei from different neuronal populations of the Drosophila brain. Using microfluidic multiplex PCR and sequencing (mmPCR-seq), we determined gene expression and A-to-I RNA editing levels at editing sites across nine distinct neuronal sub-populations and a pan-neuronal control.

ORGANISM(S): Drosophila melanogaster

PROVIDER: GSE113662 | GEO | 2019/01/18

REPOSITORIES: GEO

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