Taken collectively, ReHo investigation gives insight into coherent local connectivity of a functional cluster and is necessary for further interpreting functional changes in SAD patients, whilst the combination with SVM identifies more distributed and subtle ReHo changes helpful in characterization at individual level therefore yielding results with great potential in clinical translation.
In order to further interpret the results of the present meta-analysis, it is useful to examine some features of the past research in more detail and begin to tabulate some considerations for developing future studies which will avoid the flaws present in some of the past research and fill important gaps in the field.
In order to further interpret the proposed CS-NOMA scheme with the LCS signatures satisfying Theorem 1, we introduce the restricted isometry property (RIP) [7] which is another necessary and sufficient condition for guaranteeing the recovery of the sparse signal x in the presence of noise [7, 27].
Although a selected filtering approach might already imply a certain biological relevance of the resulting variants (for example, de novo stop mutations), specific annotations are provided in VariantDB to further interpret the effect of a variant.
In order to further interpret these findings, the DASS-21 severity categories (i.e., mild, moderate, severe, and extremely severe) were explored for each defined group of women (i.e., depressed, anxious-depressed, anxious, and stressed), with the corresponding number of women who received an EPDS classification (i.e., likely depressed and unlikely depressed) (see Table 1).
Since these findings have been well articulated in previous studies, it is unnecessary to further interpret patterns in Fig. 4 by using interview data.
For example, three-dimensional protein structures and complexes require the downloading of coordinates from the PDB [1] and then the knowledge and skill to operate a standalone program to simply reproduce the view corresponding to the figure in question and to further interpret it.
The up/down-regulated genes were further interpreted in the context of Gene Ontology biological process as well as KEGG pathways (Additional file 4).
Levels in the patients' samples were further interpreted according to the time (in days) after symptom onset (D0).
