Hi All,
I have been using IGV tool to visualize my RNASeq data from a few samples by creating a .tdf file for each sample.
Now I have 100 samples from Group A, and another 100 samples from Group B. I have identified genes differentially expressed between these two groups.
Now I would like to view these genes using IGV or other tools to see the read difference between Group A and B. Can I just create 1 tdf/wig file by merging all 100 bam files of Group A, and create another tdf/wig file for Group B, then load in IGV/Genome Browser to view those candidate genes?
Many thanks,
Shirley
Yes you can, although I am not sure what you mean by 'read difference'.