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I came across an issue with fastp in paired end mode, when inputs are GZipped fastq files. No problem with the default settings, but when Merge forward and reverse reads is set to Yes, the output files with reads are in plain text FASTQ format, while datatype is fatsqsanger.gz. I tried couple versions of the tool, got the same outcome. Here is my history in Galaxy Australia: https://usegalaxy.org.au/u/igor/h/fastptest
The text was updated successfully, but these errors were encountered:
fixesgalaxyproject#6606
fastp seems to decide on the compression of the output by file
extension. So we need to write to temporary files and move to the
tool outputs at the end for `merged*`, `unmerged*`, and `unpaired*`
outputs.
I came across an issue with fastp in paired end mode, when inputs are GZipped fastq files. No problem with the default settings, but when Merge forward and reverse reads is set to Yes, the output files with reads are in plain text FASTQ format, while datatype is fatsqsanger.gz. I tried couple versions of the tool, got the same outcome. Here is my history in Galaxy Australia:
https://usegalaxy.org.au/u/igor/h/fastptest
The text was updated successfully, but these errors were encountered: