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Finally, the gene models were manually corrected after carefully checked the alignment between SmMYB genes and MYBs from other plant species.
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Data processing was performed using an automatic processing method with a traditional integration algorithm after which each chromatogram was manually corrected to maintain the same intervals of integration for all the samples.
After automated image segmentation, the resulting labels were manually corrected to ensure anatomic accuracy.
These were then manually corrected.
Chronopotentiometry (i~t) data were manually corrected for iR loss.
The entire cortex of each participant was visually inspected, and segmentation inaccuracies were manually corrected.
Qualisys data were manually corrected, and then processed to complete any missing data.
The spectral phase and baseline were manually corrected.
The color-swap hybridizations were manually corrected to make them comparable among other samples.
Successful coregistration was visually verified and manually corrected if necessary using PMOD (PMOD 3.4, Zurich, Switzerland).
The resulting alignment was then manually corrected.
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