Hi Clarence,
Thanks for the great tool!
When running RNAforest, I set the parameter annotate =35, bt.pl.lp_genes(sdata_filter,annotate=35), the labels sticked together so that it is very difficult to make out clearly.
So if I want to obtain the top 10 genes ranked highest for each of the five localization patterns(nuclear, nuclear_edge, cytoplasmic, cell_edge and none), how should I do it?
Thank you for your help.
Best,
Melody
Hi Clarence,
Thanks for the great tool!
When running RNAforest, I set the parameter
annotate =35,bt.pl.lp_genes(sdata_filter,annotate=35), the labels sticked together so that it is very difficult to make out clearly.So if I want to obtain the top 10 genes ranked highest for each of the five localization patterns(nuclear, nuclear_edge, cytoplasmic, cell_edge and none), how should I do it?
Thank you for your help.
Best,
Melody