The dataset is composed of 51 samples of different strains (wt and mutants) that have been cultured in 3 different media. I have around 7000 genes after (1) filtering lowly expressed genes, (2) counts normalization, (3) variance stabilization and (4) batch correction with removebatcheffect(). This is the PCA of the vst batch-normalized values (different color depending on the media)
If I also perform a (5) step of selecting the most variable genes by filtering those with a variance of the vsd values < quartile 50 I reduce the dataset to around 3800 genes. This is the PCA:
I have been reading similar questions and I suspect that the samples from the glucose cultures are indeed outliers that are hindering the correct performance of the WGCNA analysis (is that probably the reason of the high power values for the model, right?). When generating the modules with power 26 I also get two large modules that are highly correlated (negative and positively) with the glucose vs. all condition (I suspect that it is also caused by those samples being much more different to the rest). Should I perform the co-expression analysis without considering the glucose samples?
My concern is that we re mainly interested in the co-expression network of one specific gene that is significantly repressed in the glucose conditions (hence being much more expressed in the non-glucose conditions). We are interested in detecting which genes are co-expressed with this specific gene, so I initially thought that it was important to keep both glucose - non glucose conditions to being able to detect the genes that have the same repression/induction pattern. Won't I lose information if I just use the cellulose-no carbon conditions in which this gene is generally equally expressed? Will I be still able to generate a co-expression network of a module that includes this gene?
Another idea was just to calculate the pearson correlation matrix of the genes dataset based on the normalized vsd values, select those genes that have >0.8 or <-0.8 correlation to my gene of interest and then perform the enrichment analysis with these lists to get an idea of the pathways/terms that are correlated to the gene. However, I initially thought that the WGCNA was a more informative approach.
Thank you so much.