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In essence, MER can be applied to any environments that deal with the execution of (scientific) workflows of many precedence-constrained tasks although MER best suits for the IaaS cloud model.
Finally, in our in-press Nature Immunology paper, we show that phagocytosis of apoptotic cells by macrophages that exclusively express Mer can be stimulated by both Gas6 and Protein S, whereas phagocytosis in macrophages that express exclusively Axl can only be stimulated by Gas6.
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Like Sars, Mers can be transmitted through the air and appears to spread particularly well in healthcare settings – most confirmed cases of human-to-human transmission have occurred in hospitals.
The dynamically linked MERs can be selected for manipulation using an interactive selection affordance.
Oligomers of length greater than 40 mers can be formed in reactions where the activated monomer is added daily to a primer.
Reads with high-abundance or unique k-mers can be removed or trimmed before performing sequence assembly (Swan et al., 2011).
K-mers can be calculated in O(n), but motif discovery is NP complete [65] and it is likely that IT features are probably at most O(n 2).
The frequency of each k-mer can be calculated from the genome sequence reads.
In our current approach, each w-mer can be considered a symbol.
A k-mer can be treated as a unit of information.
The inhibitory effect by phosphorothioate oligodeoxycytidine 36-mer can be about 200-fold greater than that by the phosphodiester oligodeoxycytidine 36-mer.
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