hello, JiekaiLab team
A grateful software for us to research TE. We can see scTE can be used to quantitate TEs reads base on Bulk RNA-seq data with the setting -CB False -UMI False. My question is if the scTE output value needs to correct with EDASeq software?
hello, JiekaiLab team A grateful software for us to research TE. We can see scTE can be used to quantitate TEs reads base on Bulk RNA-seq data with the setting -CB False -UMI False. My question is if the scTE output value needs to correct with EDASeq software?
Thank you very much!
Kui Duan