Hi all,
Sorry for what may be a very elementary question. I've been using DAVID to analyze a bunch of Uniprot IDs, with what appears to be a decent amount of success. However, I've encountered an ... inconsistency in my readouts that confuses me.
My list contains 14 IDs, all of which seem to have been read without problems by the DAVID list manager. When I go to my annotation summary results, it says that 10 of 14 showed some sort of pathway relevance. Okay, cool, that makes sense.

But when I click, I see that 7 of 14 factors were not included in the analysis? And when I go through the pathways individually, I see that that's correct -- 7 appear, and 7 do not. So what happened to the other 3? Where does the 10 come from?
I'm very new to this type of analysis, and could use a little advice from the more experienced. Thank you!
2 answers
I can see lot of posts about DAVID got updated recently, therefore I tried to compare DAVID 6.7, DAVID 6.8-beta, GeneSCFv1.1, Enrichr and REACTOME web tool for Reactome pathways.
I can find consistency in detecting number of genes with GeneSCF, Enrichr and REACTOME web tool. But DAVID gives strange results with both the versions. I thought since DAVID 6.8 beta has recently updated, it should give more accurate and updated results.
For comparison purpose I used these Cell Cycle related genes inaddition with some random genes as input to all these tools. GeneSCF_run_log
Please your suggestions are welcome, if I missed some information on DAVID update.
Here are the results..
More post on Biostars about GeneSCF,
Gene Set Clustering based on Functional annotation (GeneSCF)
Hi,
Please, I am new here and not a great bioinformatician. In DAVID tools, I have runned a list of 1500 genes in the morning and it gave a GO list of genes and in the pathway analysis it shoed Kegg, BIOCARTA and Panther...afterwards, the same list runned in the afternoon, it gave a different list of GO terms and in the pathway analysis the PANTHER list is no longer there. This has happened more than once. Would this be a result of peak time of DAVDI tool use? COuld anyone comment? T
Thank you.
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