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Hello, thanks for your great work with this pipeline. I was trying to use the fastq_dir_to_samplesheet.py script to create the sampleSheet for me but it doesn't seem like it can a directory structure in which each folder contains the paired-end reads fora sample.
How I am running the script. I provide the top directory in which all the sub directories are contained
$ ./fastq_dir_to_samplesheet.py /01.RawData samplesheet.csv --strandedness reverse
WARNING: No FastQ files found so samplesheet has not been created!
Please check the values provided for the:
- Path to the directory containing the FastQ files
- '--read1_extension' parameter
- '--read2_extension' parameter
I also saw on line 100 that recursive is set to False, but I tried changing it to true and still got nothing return sorted(glob.glob(os.path.join(fastq_dir, f"*{extension}"), recursive=True))
Any help with this? Thanks!
Command used and terminal output
No response
Relevant files
No response
System information
No response
The text was updated successfully, but these errors were encountered:
Update: I seemed to have made it recursive by changing line 100 to this return sorted(glob.glob(os.path.join(fastq_dir, f"**/*{extension}"), recursive=True))
Cheers
Description of the bug
Hello, thanks for your great work with this pipeline. I was trying to use the fastq_dir_to_samplesheet.py script to create the sampleSheet for me but it doesn't seem like it can a directory structure in which each folder contains the paired-end reads fora sample.
What my directory looks like
How I am running the script. I provide the top directory in which all the sub directories are contained
I also saw on line 100 that recursive is set to False, but I tried changing it to true and still got nothing
return sorted(glob.glob(os.path.join(fastq_dir, f"*{extension}"), recursive=True))
Any help with this? Thanks!
Command used and terminal output
No response
Relevant files
No response
System information
No response
The text was updated successfully, but these errors were encountered: