Closed diego-rt closed 2 months ago
Hi,
Thank you for the suggestions. I think you can use your own sorted BAM with the '--skip_read_alignment' in Inspector. Basically you will need to:
This should work for your case. Pleas let me know if you have met ant problems with this.
Thanks.
Hi,
Because of my genome size I need to specific the minimap2 -I parameter to a larger number. Is it possible to simply provide Inspector with the bam file rather than with a fastq file? It also would make things way easier when working on a cluster where I can distribute the mapping jobs.
Thanks!