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Is there a way to specify a common reference genome and run the analysis without protospacer #43
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Hi @npatel-ah, |
I have added a new parameter |
Thank you so much for accommodating the change. |
Hi there, appreciate these changes as this is my exact use case, but I've found that I'm getting errors when I specify both options in v2.1.1. I have tried multiple combinations of specifying When I use only When I use
Appreciate any help you may have! |
Hi @benemead, thanks for reporting this! I will open a new issue to not lose track and have a look at the bug. |
Description of feature
Hello,
This is a great pipeline, I have a feature request, which I believe is simple, I have multiple samples, with the same reference genome, now providing reference genome within the sampleshseet.csv creates a separate reference.fasta for each of them with the sample name as contig_id. Now when Minimap2 maps the Fastq to the references, all my bam files have different contigs, making it bit difficult to compare.
Also, I see the a large portion of the pipeline can be run without "protospacer" , would it be possible to make it optional ?
Best,
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