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The electrical properties of the free-form modules are parallel with the results that have been reported when similar device structure is fabricated using a rectangular design where the module is formed by striped cells [8, 19].
To calculate the fitness under one environment, a single value for each module is formed by averaging the states of the nodes contained in the module.
A miRNA-mRNA regulatory module is formed by using a bipartite graph representation [ 25], in which all the mRNAs in these rules comprise the mRNA partite, while the miRNAs are placed at the miRNA partite.
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In this approach, a co-expression module was formed for each gene included in the analysis, by identifying the 1 to 39 other genes with expression patterns that were most similar.
Finally, seven modules are formed for different MEC models to meet different user requirements.
Modules were formed from a range of standard biopolymers, including collagen, Matrigel™, and agarose, without the complex equipment often used in encapsulation.
Modules were formed by mixing NIH 3T3 cells (1×106 cells per mL of neutralized collagen) with a solution of neutralized collagen (concentration 3 mg/mL, pH 7), and then loading this mixture of cells and gel into the holes (with diameters 40 – 1000 μm) in the PDMS membrane.
Earlier observations suggested that paralogous modules were formed in massive duplication events.
Owing to the way modules are formed in Wigwams, modules with large overlap will also have similar expression profiles.
Gene modules are formed by unsupervised clustering of genes of the hierarchical cluster tree based on the threshold of dissimilarity, 1-TOM.
Modules were formed based on one of the exercise conditions, and the extent to which the module was preserved was calculated for a different condition in order to identify any reciprocal disruption of gene expression.
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