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Predicted cellulase-encoding ORFs from six clones expressing cellulase activity along with complete or nearly complete cellulase gene ORFs identified from pooled library sequencing were selected for subcloning.
Regions for sequencing were selected to capture informative polymorphic sites, based on the data from SeattleSNPs.
The recombination rate in A. gambiae was reported to be low, about 1 centimorgan per megabase [29]; and 3) the clones for EST sequencing were selected randomly.
Clones for sequencing were selected based on PCR screening.
Subjects for GCK sequencing were selected using the criteria outlined above.
A total of 50 unigenes generated by 454 sequencing were selected for experimental validation.
Similar(43)
Probe sequences were selected using a score-based selection algorithm, as described.
Three different blending sequences were selected to prepare the nanocomposites.
Target sequences were selected in silico using the gRNA design website "focas 26.
After affinity maturation only scFv with the founder sequence were selected from secondary repertoires.
Seventeen OmpA based peptide sequences were selected and analyzed based on their hydropathy index profiles.
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