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However, an attempt has been made to cluster patients into pathogenic groups based on the profile of blister fluid protein expression.
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This process is repeated until no further improvements can be made to cluster tightness.
No attempts were made to cluster findings on any other type of information.
Our results indicate that RNA-seq expression profiles in the human tissues studied here appear relatively consistent in the sense that they can readily be made to cluster according to tissue with only light preprocessing.
In summary, it seems that whatever improvements that have been made to the cluster identification algorithms are still insufficient to handle low-diversity library processing.
In this paper, an attempt has been made to propose a clustering methodology based on adaptive resonance theory (ART) for addressing these issues.
However, few attempts have been made to compositionally compare clusters of acquired genes, in order to indicate common donors, analogous to assigning donors to sequences from metagenomic libraries.
Many attempts have been made to form subgroups or symptom clusters of NPS [ 8– 12].
Numerous efforts have been made to predict CRMs comprising of a cluster of TFBSs (Berman et al., 2002), or to use cluster-based analyses to assist TFBS prediction.
To our knowledge, two previous attempts have been made to subgroup patients with LBP using cluster analysis [ 34, 35].
More recently, several attempts have been made to classify neurons quantitatively, using unsupervised clustering methods.
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