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In both early and late samples the sequence within epitope 1805-1824 corresponded to the prototype sequence (Table 2).
In order to screen for the presence of any other microbial organisms in the experimental samples, the sequence reads were also mapped against viral, bacterial and archaeal genome databases.
For all samples, the sequence of the obtained amplicon could be assigned unequivocally to the correct species by comparing the nucleotide homology in the NCBI database (BLAST, highly similar sequences).
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In addition, the resolution of these curves is controlled by sub-sampling the sequence of rings.
Once the EOS token is sampled, the sequence is considered finished (Fig. 2).
During the sequence optimization step, a Monte Carlo simulated annealing search is used to sample the sequence space.
For each sample, the sequencing reactions were prepared with forward and reverse primers in a MegaBACE 1000 DNA System.
The molecular sampling included the sequence data from Espert et al. (2007).
Further to graph structure, the attributes of the sample and sampled sequence reads can be used.
With such samples the protein sequences are usually fragments and the source organism is unknown.
In Nyquist sampling, the sample sequence x nT) contains all the information about r(t).
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