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A common workflow involves genome-wide identification of target genes, followed by transcriptomic analysis to detect fruit- or ripening-specific differentially expressed genes before conducting quantitative reverse transcription polymerase chain reaction (RT-qPCR) validation across different cultivars

Weiderpass, E., Braaten, T., Magnusson, C., Kumle, M., Vainio, H., Lund, E

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Pflanz CP, Tozer DJ, Harshfield EL, Tay J, Farooqi S, Markus HS