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To identify infections by multiple variants, five clones from each transformation were selected for sequencing analysis.
In order to compare expression levels of the PvUbi1 and PvUbi2 promoters with those of other promoters, several plant promoters commonly used in monocot transformation were selected and cloned into the same identical vector (pHLucGWgus) to eliminate any discrepancies in expression levels as a result of vector backbone or vector size (Additional file 1, Figure S2).
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After transformation, transformants were selected on agar containing tetracycline (12.5 μg/ml).
The optimal transformation is selected by the most votes.
In rough localization, the best transformation is selected from four transformations.
The convenient techniques for a joint power spectrum transformation are selected.
The best transformation is selected as the one yielding the best QLCP measure and then further refined with the ICP algorithm.
A single colony from each transformation was selected to begin the mutation accumulation experiment.
The shape of the transformation was selected prior to modelling and not altered in light of its results.
Line K used as parental line for genetic transformation was selected as a control for comparative purposes [ 9].
This transformation was selected to stabilize the variance of the cycle; the magnitude of the variation was greater when the BLLs were higher in the earlier years.
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