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Since the mutants were arranged in 96-well plates randomly, outliers on each plate were identified as normalized O.D. readings that deviated significantly from the average on each plate.
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Moreover, we found that the bulliform cells are arranged with "U" shape in WT, whereas the bulliform cells of rel2 mutant are arranged with "V" shape (Fig. 3a, b).
The mutant strains were arranged in quadruplet to create a dilution in a given square giving a total of 96 strains plated per agar plate.
The experiments used to determine the populations of the EB (Rif +) mutants and the pathogen were arranged in a completely randomized block design consisting of three replicates, with one plant per replicate.
The mutants identified in the 1st round screen were arranged into pools of ∼30 mutants for a 2nd round screen in both the chinchilla and mouse models as described above.
However, in the Foxc1 null mutant (D, D′ ), the PCs were arranged as clusters within the anlage (D′, asterisk).
A total of 5,280 STM strains were arranged in 96 mutant sets (∼55 mutants/set) based on the identity of the sequence tags to prepare the input pools.
However, in the CAAS mutant population, the two copies of 35S enhancers were arranged next to the RB of pER38.
But compromises were arranged.
Appendages were arranged on tables.
Few were arranged into verses.
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