Entering edit mode
5.5 years ago
Neu
▴
10
Hi, I have read count of circRNA junctions obtained by analyzing RNA-Seq data. How can I merge these files to calculate fold change using DeSeq2?Some sample may contain junctions that are not detected in other sample or replicate analysis and I need to put zero in that condition. Any help will be appreciated. .
Have you tried
full_join()
fromdplyr
?DESeq2 has several features for importing data: did you give a look to them? You can find them here