Hello,
The FASTQ Joiner tool is currently being updated to work with the newer
sequence Id format. The progress of this change can be tracked here:
https://bitbucket.org/galaxy/galaxy-central/issue/677/update-joiner-tool-to-work-with-casava-18
Meanwhile, quality filtering can be done on each
Hi,
I have HiSeq2000 paired end sequence data in two separate FASTQ files.
I need to filter the low quality scored sequences from my data to have a
good assembly. So I decided to join the PE reads and then filter the low
quality sequences in Galaxy.
To do this first I groomed the data using
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