Hi All,
I have a quick question. I am struggling to understand how the RT similarity function of MSDIAL is working. Do we need to use the same gradient explained in `A lipidome atlas in MS-DIAL 4` article?
If we didn't use the same gradient does it make any sense do use the Retention time similarity function?
Have all the retention time data embedded to `Msp20210527163602_converted.lbm2` from the paper?
Thanks for your help!
Cheers.
Cagakan