Hi, Akihiro
I met some problems when I try to use DAJIN in a benchmark between different nanopore genotyping methods.
1) I run your method on the server and I don't have the sudo permission so I can't update conda by conda_setting.sh. Thus, I create Nano. sim and DAJIN environment on my own following your requirements but it still met problems when I run the main program, the conda environment cannot be initialized. I tried to run your script separately but it failed. and I could not solve the problem by removing conda_setting.sh. are there any suggestion to solve this problem?
2) my datasets are nanopore-sequenced CRISPR results for certain single gRNA . so what is the difference between WT and target in design.fasta file if I have no external oligos insertion
thank you for your help and time
Hi, Akihiro I met some problems when I try to use DAJIN in a benchmark between different nanopore genotyping methods. 1) I run your method on the server and I don't have the sudo permission so I can't update conda by conda_setting.sh. Thus, I create Nano. sim and DAJIN environment on my own following your requirements but it still met problems when I run the main program, the conda environment cannot be initialized. I tried to run your script separately but it failed. and I could not solve the problem by removing conda_setting.sh. are there any suggestion to solve this problem?
2) my datasets are nanopore-sequenced CRISPR results for certain single gRNA . so what is the difference between WT and target in design.fasta file if I have no external oligos insertion thank you for your help and time