Hi,
I'm trying to finetune the model using whole genome-wide methylation sites. I read about your suggestions in #4 , and I'd like to try that. But I have one more question related to the input of the model. I'm wondering if it is possible to add some new channal(s) which contains data from ATAC-seq, ChIP-seq or other epigenetic sequencing methods as the input. If it's possible, could you give some suggestions on this?