I have some Illumina reads and Nanopore reads I'd like to assemble using Unicycler. I uploaded the raw fastq files, groomed them, and ran Unicycler on these with the default settings. I received the following error: "Remote job server indicated a problem running or monitoring this job." Does this sound like a Galaxy problem or a problem that I can solve? Any help is greatly appreciated! Our Linux computer is not connected to the internet so I'm having trouble getting programs installed there and I'm stuck with a Windows for the time being, but alternative assembly methods are also greatly appreciated!