yonniejon
yonniejon
Thank you!!! very helpful
If this is still a problem, post an update and re-open.
Hi, for generating bam files from fasta files you should use an alignment tool like bwa-meth or bismark on a fasta file. For clustering there is not best option, but...
Yes, use the init_genome command and provide your own fasta file --fasta_path /path/to/genome.fa
Also, there is a bug I think when I do share-y the y-axis label uses the max value of the overlayed track even though the actual value is the original...
does `wgbstools set_default_ref hg38 ` work?
yes bam2pat same as a bam file!
Are you using the files downloaded from the paper? I believe these files are using the hg19 reference genome while you called --genome hg38 in your command. Let me know...