Entering edit mode
Hello,
I have human lung cancer cell data with no replicates, and following all the procedures in DESeq2.
After rlogTransformation, I got this table:
rld<-rlogTransformation(dds2),
X549_repair.bam | X6_repair.bam | X6plus_repair.bam | X14_repair.bam | X14plus_repair.bam | |
ENSG00000223972.5 | -0.705380592 | -0.7948932821 | -0.7949855462 | -0.7503978596 | -0.7932775487 |
ENSG00000227232.5 | 6.1414437565 | 6.2217508536 | 6.2959599684 | 6.0194334914 | 6.2919290386 |
ENSG00000278267.1 | 1.6994131779 | 1.732395436 | 1.9045910114 | 1.73851203 | 1.925247887 |
My question is: is that possible I can calculate the foldchang of two samples just use this table?
Thank you in advance!