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Calculated low-frequency vibrations of AsnSm clusters demonstrate that the collective torsional and out of plane bending vibrations of the big 10- and 12-membered rings (10.8 and 9.0 cm−1, respectively) and torsional vibrations of As2+4/3S5 branched AnSm clusters (12.8 can1) contributebuto to g/ω 2 (Fig. 6) and k(T) above the plateau in g-As2S3 (Fig. 4).

Further, the GO terms were distributed throughout the clusters, demonstrating that genes that are coexpressed are from diverse functional groups.

Surprisingly, PEGylated NPs with no active targeting moieties also accumulated in these clusters, demonstrating that the nanoscaled carriers passively accumulate in clusters via a mechanism similar to that for the enhanced permeability and retention effect, as has been well established in tumor targeting.

Further examination of the DHSS clusters demonstrated that the VPA-induced DHSSs have different characteristics compared to non-induced DHSSs.

There is a high degree of separation among the clusters, with an average correlation of 0.026 between all of the clusters, demonstrating that the expression profiles for genes within a cluster are not similar to expression profiles for genes in other clusters and thus each should be considered separately in this study (see Methods).

An analysis of several MD simulation runs on both the FDM and a standard PC cluster demonstrates that the FDM's interconnect architecture provides a greater performance compared to a more general cluster interconnect.

Metabolism-based hierarchical clustering demonstrates that the R. bieti, dog, chicken, human and pygmy loris samples clustered together and separated from those of the mice and cow.

This is the first functional information about the swf cluster, demonstrating that the predicted ACP domain folds correctly, is recognized by PPTase, and is therefore presumably functional.

Hierarchical clustering demonstrated that the expression of TAM markers, CD68 and CD163, is more closely associated with the expression of SOX2).

There were 15,239 DMLs between the 2 clusters, with 8,324 hypermethylated and 6,915 hypomethylated in cluster 2. Hierarchical clustering demonstrated that the 15,239 DMLs could be used to distinguish between the 2 clusters.

Visualization of these differentially expressed genes by hierarchical clustering demonstrated that the expression patterns of the corresponding experimental groups for both RASFsn-stimulated and NDSFsn-stimulated chondrocytes were similar to each other; corresponding groups clustered and showed little degree of variability.