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Fusion was conducted as described above except that the GFP and puromycin resistance markers were swapped.
That is, any possible bias was not strong enough to show a significant difference when the markers were swapped.
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Religious textbooks were swapped.
Parts were swapped out, rescued, jerry-rigged.
Securities were swapped for loans.
Rounds were bought, stories were swapped.
Trees were swapped using the TBR algorithm.
Dyes were swapped between different pairwise comparisons.
All trees were swapped by random stepwise addition with TBR branch swapping.
In the second hybridisation, the dyes for labelling were swapped.
The KanMX marker in CKY1026 was swapped for NatMX using homologous recombination to make CSY158 (Goldstein and McCusker, 1999).
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