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Results showed that microorganisms in the GAC packed MFC could be assigned into four groups, consisting of Alphaproteobacteria, Betaproteobacteria, Bacteroidetes and Acidobacteria (Figure 1).
4 986 METTL3- and 922 WTAP-binding clusters were enriched and could be assigned into four RNA categories: mRNA, miRNA, large intergenic non-coding RNA (lincRNA) and pseudogene.
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The patients will be assigned into two groups.
Both parameters suggested that the 472 genotypes could be assigned into three groups.
These differentially expressed genes could be assigned into seven groups based on the comparison of the expression level in hybrids and their two parents (Table 1).
As a result, 724 (78.52%) TUSs could be assigned into three principal categories: molecular function (599), biological process (559), and cellular component (570).
Among these 3698 TUSs, 2106 could be assigned into three major categories: (i) molecular function, (ii) biological process and (iii) cellular component.
The values of t* for the other criteria can be assigned into two bands, both of which differ quite substantially from 30.
When seven was taken as the cutoff value, a total of 88 genes or possible operons, which could be assigned into nine functional categories, were picked out as the potential direct PhoP targets (see Additional file 10).
Quantified parameters (e.g. a/b, a/c, coordination number) from the geometry and network models extracted from FIB and TEM images at the nanoscale are assigned into four pore associated phases in PFIB images.
Based on these three sequential stages of class prediction, samples were assigned into four independent prognostic subtypes (BEST, GOOD, BAD, and WORST) as follows.
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