yonniejon

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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...

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...