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Measuring RNA editing through mmPCR-seq in Drosophila adapting to divergent microclimates and raised at different temperatures

ABSTRACT: We applied microfluidic multiplex PCR and deep sequencing (mmPCR-seq) to quantify RNA editing levels at targeted sites in 32 isofemale lines from two divergent microclimates at 'Evolution Canyon' in Israel (16 fly lines from each microclimate). Editing levels were compared between different populations at 25˚C , and were also compared between 25˚C and 18˚C within populations.

ORGANISM(S): Drosophila melanogaster

PROVIDER: GSE104084 | GEO | 2017/09/20

SECONDARY ACCESSION(S): PRJNA408169

REPOSITORIES: GEO

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