Closed search42 closed 10 months ago
Can you report the command line used to fix your files?
Can you report the command line used to fix your files?
Thank you for such a quick reply. After the data is mounted, run the following command in the image:
set -eu -o pipefail cd ${out-dir} ln -s /fastqwiper/bbmap /fastqwiper/pipeline /fastqwiper/run_wiping.sh ${out-dir} mkdir -p ${out-dir}/data ln -s ${read1-input} ${out-dir}/data/${sample-id}_R1.fastq.gz ln -s ${read2-input} ${out-dir}/data/${sample-id}_R2.fastq.gz perl -i -pwe 's#cd /fastqwiper##' run_wiping.sh bash run_wiping.sh paired 8 ${sample-id} 50000000
OK, I'm afraid I need to use your fastq files to debug fastqwiper. Can you send them to me?
To debug the software we really need to use your files. Can you share them?
To debug the software we really need to use your files. Can you share them?
I'm sorry, but I can't share it with you because of the data privacy policy. If I'm having the same problem with public data, I'd be happy to share it with you
Please share them or link
If you can share any file that causes this error, please reopen the task
I encountered an issue with a paired-end fastq data. I attempted to fix my data using the image mazzalab/fastqwiper:2023.2.82 and the fix_wipe_pairs_reads_parallel.smk within it. The software fastp can handle the output data properly, but when aligning the resulting files of the software fastp to a genome using BWA, an error message appeared: :
I examined the fastq data produced by the fix_wipe_pairs_reads_parallel.smk workflow and indeed found such problems:
The same issue also appears in the output paired-end reads of fix_wipe_pairs_reads_parallel.smk