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The proportion of methylated templates was then quantified according to methodology previously described [ 111].
This sequence of 3 templates was then fitted back to the 9 individual recordings.
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Wood templates were then prepared from the scrive board and steel plates marked off and cut to size.
The templates are then converted into solid microcapsules with a matrix structure by solvent evaporation.
These templates are then validated using information from the History Database and Constraints Validator.
The AAO templates were then removed by immersion in 1 M NaOH solution overnight.
Both cancelable templates are then merged together using concatenation-based feature level fusion technique [20] to generate a combined template.
These templates are then used in demodulation, resulting in a low-complexity non-coherent alternative to complex Rake receivers.
These templates are then arranged in order, given the right twist angles, glued and screwed to form a whole blade template.
Templates were then PCR screened to identify individual clones containing the gene of interest.
These two sets of templates were then, in a semi-automatic way, matched to the recorded force (taking into account the instantaneous muscle length to interpolate across noise templates), and the two sources of noise were then subtracted off sequentially.
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