Re: Fwd: WGCNA: labeledHeatmap and verboseScatterplot correlations and p-values are not the same
Sindre Lee <sindre.lee-/[email protected]>
| Newsgroups | gmane.science.biology.informatics.conductor |
|---|---|
| Message-ID | <[email protected]> |
Thank you for your answers! Please see inline for a final comment. On 2014-08-11 19:47, Peter Langfelder wrote: > Hi Sindre, > > please see inline. > > On Sat, Aug 9, 2014 at 9:47 AM, Sindre Lee <sindre.lee-/[email protected]> > wrote: >> Thank you! I understand now, its actually well described on the >> webpage and >> in the documentation, I should have used more time reading before >> posting. >> >> If you have the time, I actually have a few more questions: >> >> 1. Why is the module size set at min. 30? What will the implications >> be if >> larger/smaller? > > I feel that 30 is a good compromise between robust large modules and > possibly informative but not as robust small modules. You can > certainly adjust the minimum size, although I rarely find modules > below 30 genes interesting. The implication is very simple - smaller > minimum module size will lead to more modules, but whether this > provides more biological information or just more noise is highly > situation-dependent. > >> >> 2. Is it always better to use the step-by-step network construction >> and >> module detection? > > The step-by-step gives you more options to tweak the procedure or > insert your custom code between the steps. Otherwise they are (nearly) > identical. I say nearly because the blockwise... functions include an > extra step of removing peripheral genes from modules. > > > >> Let me give you some details of my design so you >> understand why I ask. I have two time points, from the same persons, >> before >> and after an intervention. My immediate idea was to run WGCNA on the >> time >> point 1, relating it to body weight. Then I run WGCNA on time point >> 2, >> seeing if the same modules pops up. Finally, I run WGCNA on the >> log-ratio ( >> time point 2- time point 1 ) against log-ratio of body weight. If one >> or >> more modules shows up in all three runs, they will be prioritised. >> Now, if I >> only use the one-step approach, no modules show up in all three >> comparisons, >> while using step-by-step looks more promising. However, if I mix the >> results, using one-step on time point 1, but step-by-step on time >> point 2, >> its even more interesting. > > > If you want to see modules that pop up in all 3 data sets, use the > consensus module approach. But it's not clear to me that looking for > modules in data set 1, data set 2, and the log-ratio of the two makes > sense. You could get consensus modules across sets 1 and 2, and then > see if the log-ratio of interesting modules is still associated with > the log-ratio of body weight. Ok, I will try that, thank you! My thought was that if the module was related weight (in two data sets) and changes (log-ratio) in weight, wouldn't that point to a stronger relationship? If not, why? _______________________________________________ Bioconductor mailing list [email protected] https://stat.ethz.ch/mailman/listinfo/bioconductor Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor