You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Hi! Thanks for a great tool. I was wondering if you could implement an option to remove a contig or a list of contigs when calculating the stats. Sometimes I have bacterial contaminations, or the mitochondrial contig has crazy coverage compared to the chromosomes, so I fear those values might inflate upwards the average depth of coverage in the report. Rather than re-map the reads to a reduced reference genome, I think it would be great if Cramino could consider it if asked.
Thanks!
The text was updated successfully, but these errors were encountered:
While I haven't added this yet, I would just like to point out that you can use samtools to filter the file and pipe that into cramino to read from stdin. That should get you what you want.
Hi! Thanks for a great tool. I was wondering if you could implement an option to remove a contig or a list of contigs when calculating the stats. Sometimes I have bacterial contaminations, or the mitochondrial contig has crazy coverage compared to the chromosomes, so I fear those values might inflate upwards the average depth of coverage in the report. Rather than re-map the reads to a reduced reference genome, I think it would be great if Cramino could consider it if asked.
Thanks!
The text was updated successfully, but these errors were encountered: