(product length 90–300) based on the CDS sequences of the corresponding genes and subsequently verified the stability through semi-quantitative RT-PCR and RT-qPCR. A total of eight primer pairs were selected for subsequent experiments. Eight internal reference genes were ribosomal protein S30 (...
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a sequence-based m6A modification site predictor. Integrating the prediction results and data in Fig.4e, we identified two potential m6A modification sites with very high confidence: site 602 A in the CDS region and site 820 A in the UTR region of theFDX1transcript (Fig.4f,...