Hi, I'm trying to solve an issue I'm having with my local installation of
Galaxy (installed on my own computer, rather than on a server). I'm using
data in the form of fastq files from an Illumina Hi-seq and I want Galaxy
to parse the bar coded sequences out into individual files for me. I've
been using the public server in the past, and I'm able to use the Groomer,
Joiner, Reverse-Complement, Trimmer, and Barcode Splitter tools just fine.
Now I'm trying to do the same thing locally on the same files. Both the
large file (38 GB) and a smaller file consisting of the first 10k lines
will upload just fine. However, I can only get the Groomer to work on the
small file. When I use it on the large file I get an error: "Error
executing tool: maximum recursion depth exceeded while calling a Python
Any help on this would be greatly appreciated!
- Chris M.
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