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More Sensurround systems were assembled and installed.
The sequences obtained from Miseq were assembled using the CLC genomic workbench (CLC Bio, Denmark), and the sequences from the 454 sequencing systems were assembled using GS De Novo Assembler 2.3 (Roche Diagnostics, Branford, CT).
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Fourthly, the team of hub-beam systems is assembled.
Such systems are assembled with angle brackets and hold-downs, anchored to the wall and floor panels with profiled nails and bolts.
The fully coupled systems are assembled and solved in parallel using the Single Program Multiple Data (SPMD) paradigm with one layer of ghost cells.
This review discusses various mechanisms by which polymer systems are assembled in situ to form implanted devices for sustained release of therapeutic macromolecules, and highlights various applications in the field of advanced drug delivery.
These secretion systems are assembled into six major groups, named types I, II, III, IV, V and VI (Thanassi and Hultgren, 2000; Henderson et al., 2004; Mougous et al., 2006).
In this review, we discuss various mechanisms by which polymer systems are assembled in situ to form implanted devices for sustained release of therapeutic macromolecules, and we highlight various applications in the field of advanced drug delivery.
The sequences of Jalo EEP 558 from the Roche 454-FLX system were assembled using the software 454 GS de novo assembler, Newbler from Roche Applied Science to generate the Jalo EEP 558 reference sequence.
The 96,169 reads (range: 40 680 bp) of P. verticillata cpDNA generated by the 454 system were assembled against the reference sequence of Chionographis japonica (Bodin et al. 2013).
A two-channel flow system was assembled.
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