Hello Everyone,
I used P2 Solo to perform genome sequencing on 21 bacterial strains. I applied the "--one-to-one" option of the pod5 conversion pipeline to convert hundreds of fast5 files to pod5. I then carried out basecalling and demultiplexing (I'm working on WSL).
dorado-1.1.1-linux-x64/bin/[dorado][1] basecaller --no-trim hac /mnt/c/data/bacteria/pod5_out > --output-dir my_output
dorado-1.1.1-linux-x64/bin/dorado demux --kit-name SQK-RBK114-96 --emit-fastq --output-dir demux_out calls.bam
The issue is that we worked with 21 barcodes (5 to 25), yet I received 96 fastq files in demux_out that corresponded to the 96 barcodes. Additionally, I'm unsure if I should re-trim the fastq files prior to doing any downstream analysis (e.g. Porechop).
Suggestions appreciated. Thanks
If you're using WSL, PowerShell has nothing to do with this. It also sounds like a better question for your sequencing facility/provider rather than anyone here. Are all of your actual supposed barcodes found?