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Moreover, in most cases, the connection value between a cluster and its neighbors is larger that the threshold, only one sensor in each cluster needs to be in active state.
High homogeneity indicates a bi-directional correspondence between a cluster and a complex [ 17].
This analysis can also help to rank the ontological distance between a cluster and its trans-factors according to the semantic similarity values.
To alleviate this problem, rather than calculating enrichments for genes known to be involved in EMT, we calculate the FSS that measures the degree of functional similarity between a cluster and a reference set of genes associated with EMT.
Moreover, the absolute rate of monomer uptake (that is, the swelling rate of a particle) is also higher for the absorption of single molecules, as only nsm molecules are transferred per collision between a cluster and a particle.
Roughly 40% of the severing events in our AFM observations occurred at the boundary between a cluster and a bare zone or within the neighboring bare zone, which may be explained by these hypotheses.
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When we estimated the pairwise kinships between individuals within a cluster and compared their average between clusters, the difference in average pairwise kinships between cluster 6 and all individuals was significant (Fig. 5).
The two measures reflect different features of the similarity between a clustering and a reference and we therefore included results from both (see Methods).
We observed very consistent annotations between SwissProt proteins in a cluster, because of the high sequence identity between proteins in a cluster and the reliability of SwissProt annotation.
The results reveal the connection between the formation of a cluster and the variation of energy in fluidized beds.
Cluster stability was assessed with the sum of squares error between the centroids of a cluster and its associated probes.
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