Entering edit mode
2 days ago
carolofharvest
▴
50
I am doing transcription factor activity analysis on my single cell data and I ve used lmer model for statistical comparison between my two condition.
I want to plot my results in heatmap ( TFs as rows, Celltype as columns) . I think I can use esiimate values generated from lmerTest::lmer() function as they are like fold change values but I am not sure.
Should I use estimates values on plots directly without scaling them ? If i use real estimates values ( max 0.3 , min - 1.5) , i get really weird plot.
Some might know what "lmer model" for "transcriotion factor analysis" is. Why don't you show representative data so people can suggest visualization. Maybe a link to a paper doing similar?
HI ,
This is the link of the plot (see figure K) ; https://www.nature.com/articles/s41590-024-01994-8/figures/14
Here they ve used log(medFC) , scores are calculated by using PROGENy. I ve noticed that estimate values and foldchange values can have different signs , so different direction in pathway activity; I suppose calculating foldchange is just a superficial way of showing direction compared to lmer estimates because lmer also takes into account random sample effect.
But I ve tried calculating foldchanges as they did in this article , but i dont know how they handled NANs produces after log transform (i ve tried adding pseudocount). And median scores for celltypes in different conditions are not always positive , cell types with negative scores shows downregulation of pathway , in other ways upregulation of genes that have negative weight in that pathway.
And this is the link of the article :