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All of the PFF clusters share a focus on improving the culture of academic training and the preparation of newly trained Ph.D.s.
In the top left dendrogram none of the other clusters share a common motif.
It is therefore probable that these two gene clusters share a common ancestor and arose by duplication.
We show that if the two gene clusters share a common ancestry, it dates back to the early days of eukaryotic evolution.
Although AnnSim seq clustering is composed of larger-sized clusters, e.g. clusters with 6, 8 and 10 drugs, the drugs on these clusters share a high number of categories.
We present phylogenetic evidence revealing that the phage tail-like components of the PLTS gene clusters share a common ancestor with the corresponding structural components of T6SS and R-type pyocins.
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Mass spectrometry-based analysis showed that peptides generated by endolysosomal in vitro proteolysis formed nested clusters sharing a common central core but displaying variable flanking regions.
The P-cluster can be viewed as two [Fe4S4] clusters sharing a common S atom, and the structure of this cluster is redox-dependent.
Serogroup B isolates between clusters shared a low level of PFGE pattern similarity, with no single genotype predominated among the isolates.
Two approaches that are commonly employed to reduce redundancy in large data sets are (a) assembly: where sequences are assembled into longer contiguous fragments (contigs) and (b) clustering: sequences are grouped into clusters sharing a defined degree of similarity.
However, this explanation also seems unlikely given the high average recapture rate in this study, which often led to individuals being sampled among different party associations, as well as the large distances between some sampling clusters sharing a haplotype.
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