By providing a detailed computational model, we decompose a complex mental process into a series of elementary operations governed by precise, routine instructions.
This fact is supported by providing a comparison of the computational complexities of these algorithms.
The derived metric, global selfishness, significantly relieves the computational burden by providing a simple decision rule for computing cooperative vectors in each cell.
The portal will hide the complexity of the underlying technology by providing a unified user interface making computational chemistry in general more readily available.
Although technically demanding, further experimental data on the ability of organic compounds to enter the bacterial cytosol would be of great utility by providing a structurally more diverse dataset for computational studies.
Because database development is important for further experimental and computational designs by providing a high-quality benchmark, we focus on data collection and manually curated 6897 bivalent genes in this work.
The GAME framework proposed by Nathan and Martinez (2015) provides a computational account of how actions that are initiated without specific meaning contribute to specific meaning-making through mental simulation.
Therefore, this discrepancy in the disorder prediction by CDF and CH-plot might provide a computational tool to discriminate proteins with extended disorder from native molten globules, which might be predicted to be disordered by CDF, but compact by CH-plot.
Furthermore, we emphasize the importance of this class by showing how to transform an arbitrary system into a disjoint circular wait free one in linear time and in a property preserving way and by providing various computational complexity results.
Moreover, our tool can avoid the problem of identifying the functional strand in novel miRNA precursors, where the performance accuracy of all compared tools is very poor, by providing as computational truth the miRNA:miRNA* duplex while maintaining the same high accuracy in terms of start nucleotide prediction.
