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Using MLST analysis, the genetic relatedness of Candida isolates has been assessed in two Brazilian studies of candidemia, in which different clusters have been found among isolates of C. albicans [ 24] and C. tropicalis [ 65].
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Similarly, in Eq. 5, the number of neighbor sensor nodes of different clusters has been considered (see the second parameter) that ensures better selection of a gateway node for inter-cluster communication.
Different symptom clusters have been correlated to QEEG frequency bands.
Six different gene clusters have been described (vanA-B-C-D-E-G) (6, 10– 10).
The second possibility is that the different Irx clusters have been independently acquired, implying numerous independent tandem duplications and pressures to maintain the physical linkage of duplicated genes in several different lineages.
To date, many different gene clusters have been found in this location (Hu et al. 2013; Kenyon and Hall 2013; Hamidian et al. 2014; Kenyon, Marzaioli, et al. 2014; Senchenkova, Popova, et al. 2015; Senchenkova, Shashkov, et al. 2015; Shashkov et al. 2015; Kenyon, Marzaioli, De Castro, et al. 2015).
To date, three different siderophore biosynthesis gene clusters have been described in A. baumannii [ 21- 23].
Many oxo clusters have been isolated with different degrees of condensation (a: b ratio), different degrees of substitution (a: d ratio), different proportions of residual OR groups (a: c ratio), and, as a consequence, different structures.
The sequences and fully annotated contigs representing the different type VI secretion system gene clusters have been deposited in GenBank for strain BD 442 (KF552074, KF552074), PA-4 (KF590030, KF590028, KF590028) and LMG 2665T (KF590027, KF590027).
A number of similar van clusters have been identified in different bacterial species, and whether these evolved independently or by divergent evolution is unknown.
More ancient clusters have been identified.
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