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Similar aspects of the literature that have been investigated in both papers are compared below in order to examine whether related trends have been isolated across the two sets of analyzed papers.
The two sets of analyzed themes were compared and discussed until a consensus was reached, and the themes were combined, summarized and classified accordingly.
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Taking into account the CNV genome coverage (1.2% 'polymorphic-SMC' and 2.3% 'polymorphic-DC') and the relatively small overlapping fractions (0.39 and 0.20, respectively) between the two sets of 'polymorphic' CNVs analyzed in this study, we estimated that up to 10% of the human genome is covered by highly polymorphic CNVs.
The two sets of genes were analyzed by significance analysis of microarrays (SAM) using 100 iterations in the two-class, unpaired data option [12].
Two sets of pairs were analyzed by imaging MALDI MS and MS/MS mode, respectively, at a spatial resolution of 200 µm.
To measure the expression of selected genes two sets of cDNA were analyzed: the same set of cDNA from the cells and tissues that were used during the DNA microarray hybridization experiments and another set from 12 matched pairs of normal and tumor breast tissues.
Two sets of samples were analyzed.
The two sets of experiments were analyzed separately.
Two sets of samples were analyzed: Microcystis strains and field samples.
Two sets of data were analyzed using an independent sample t test.
To assess the comparability of the two measurements, the relationship between two sets of data was analyzed by Spearman's rank correlation test.
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