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Three clones, syNP4, 13 and 34, of 112 G418-resistant colonies were selected for subsequent analyses.
Likewise, the replicates allowed sensible quality assessment and the best two arrays for each mouse tissue and three arrays for each human tissue were selected for subsequent analyses.
This second model was therefore selected for subsequent analyses.
Genes with a significant treatment effect only were selected for subsequent analyses.
Thus, the non-normalized data, with SD 2.35 were selected for subsequent analyses.
In total, 16 samples (balanced for mixing group) were selected for subsequent analyses.
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Samples with a main histological subtype (n = 66) were selected for subsequent subtype analyses.
The unigenes showing best tBLASTn scores to protein sequences functionally characterised in other species were selected for subsequent transcriptional analyses.
Similar to the ABIDE consortium paper [ 2], 794 subjects from the original participant pool were selected for subsequent imaging analyses.
Factors notably associated with the flock status at 20% level through univariate analysis (Table 1) were selected for subsequent multivariate analyses.
Various mRNA abundance patterns were observed among the dietary treatment groups (Table 1) and 5 genes were selected for subsequent confirmation analyses.
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