Hi!
I have run EasyFuse version 1.3.6 with my ~700 tumor bulk RNA-seq sample and filtered some inspiring fusion results.
It would be helpful to get the supporting reads number for each fusion result thus I can choose some to validate first.
With the released versions of EasyFuse, can I get the supporting reads in outputs?
If not, any suggestions about getting supporting reads would be grateful.
Thank you so much!
Tesson,
Shanghai Jiao Tong University,
September 18th, 2023.
Hi! I have run EasyFuse version 1.3.6 with my ~700 tumor bulk RNA-seq sample and filtered some inspiring fusion results. It would be helpful to get the supporting reads number for each fusion result thus I can choose some to validate first. With the released versions of EasyFuse, can I get the supporting reads in outputs?
If not, any suggestions about getting supporting reads would be grateful. Thank you so much!
Tesson, Shanghai Jiao Tong University, September 18th, 2023.