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Monomeric anthocyanins were quantified using the pH differential method previously described by Giusti and Wrolstad [14].
Rutin was assayed in the samples by LC according to the method previously described.
The in vitro drug interactions were analyzed according to the method previously described (Chou, 2006).
Automated analysis is performed based on the detection method previously described.
ROS production was measured according to the method previously described [5, 16].
The phenolic compounds were extracted following the method previously described (Khalid et al. 2017).
Fusion PCR was performed according to the method previously described (Kuwayama et al. 2002).
We classified the identified genes using a similar method previously described (Kang et al. 2016).
BCRP expression in HEK cells was confirmed by RT-PCR using the method previously described [54].
True count rates were estimated using the extrapolation method previously described.
Library preparation and transcriptome sequencing were performed by the method previously described (Liu et al. 2015a).
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