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Templates are then stored as the weights of "neurons".
These templates are then exported into the cell's main compartment, the cytoplasm, and made into proteins.
The templates are then converted into solid microcapsules with a matrix structure by solvent evaporation.
These templates are then arranged in order, given the right twist angles, glued and screwed to form a whole blade template.
These templates are then validated using information from the History Database and Constraints Validator.
These templates are then committed to a Git repository and from then on, the whole team works from that one repository.
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The circularized DNA templates were then randomly sheared using the Covaris LE220 (Covaris).
The SMRTbell templates were then purified using exonuclease treatments and size selected using AMPure PB beads.
Wood templates were then prepared from the scrive board and steel plates marked off and cut to size.
The AAO templates were then removed by immersion in 1 M NaOH solution overnight.
Templates were then PCR screened to identify individual clones containing the gene of interest.
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