I’m trying to use the ‘qiime2 tools import’ for SampleData[SequencesWithQuality] with ‘Single Lane Per Sample Single End Fastq Directory Format’.
I think I’ve correctly build the manifest and metada files. But I keep getting the same persistent error regarding the element ‘name’.
This parameter asks me for “Filename to import the data as. Must match regex: .+_.+_L[0-9][0-9][0-9]_R_001.fastq.gz” but it doesn’t matter which name I try it always seems to fail, so Galaxy doesn’t even execute my job.
I’ve also tried to look up RegEx matchers to know if my created name would be suitable but these don’t seem to be helpful.
Can you help me in this matter? I’m not really a coder hahaha but I really want to understand this.
p.s. everything runs perfectly when i’m using QIIME2 on command line, the problem seems to be nested in galaxy… (which I prefer because buttons)
The import function has more discussion cross posted over at the EU Matrix chat → You’re invited to talk on Matrix
The “element identifiers” are the names of the files inside the collection. When creating a collection, the file extensions are usually removed – that is why the extra option to add them back in is also listed.
Tools in the Collection Operations tool group can be used for renaming element identifiers. Is that what you are doing?
Example for using the tool when run in Galaxy. Note that the naming is more specific than command line (technical reasons…). If sample ids are included in any other inputs, the naming should be consistent.
Single-end reads in fastq.gz files where base filename is the sample id
The full file name, minus the extension (.fastq.gz) is the sample id.
- sample-42_S1_L001_R1_001.fastq.gz is sample-42_S1_L001_R1_001
Please post back a few of the element identifiers names if you would like more help. You could also post a shared history link. Troubleshooting errors
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