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Only top level clusters were selected for further analysis.
Given their spatial locations, climatic conditions, and significance with regard to population and economy, these city clusters were selected for our study.
Proteins in these core clusters were selected for k-means analysis of 27 gliomas using, as before, an 85% resampling of proteins and consensus matrix analysis over 10,000 iterations.
These modules (or gene clusters) were selected for further analyses.
Two additional clusters were selected for quality control.
Twenty one clusters were selected for data collection using structured questionnaire.
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Based on the results, suitable clusters are selected for studying lithium penetration into the oxide structure.
piRNAs are derived from specific genomic clusters, but it is unclear how the transcripts from these clusters are selected for processing into primary piRNAs and many of the processing enzymes remain to be identified (reviewed in Ishizu et al., 2012).
From this cluster analysis, two representative isolates of each cluster were selected for further analysis by 16S rRNA gene sequencing and thereafter the tentative identification was extrapolated for the entire group of isolates in each cluster.
TNFα induced up- and down- regulated genes were clustered hierarchically on the basis of their normalized expression intensities (Figure S2) and genes with the same GO functional term and within the same cluster were selected for further promoter analysis.
Five isolates from this cluster were selected for MLST analysis.
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