Quick background: I primarily do lab work and have not dabbled in bioinformatics, just started using galaxy, following this tutorial to analyse public datasets:
The fastq file is a URL from entering the SRA file number into EBI SRA (ENA). I tried using the SRA toolkit to convert to FASTQ but it was proving too challenging for my non-programming brain, and others on forums suggested using EBI instead. This was saved into my Galaxy, and when I tried to do the next step which was the FASTQ Groomer on my FASTQ file, it paused my job because the disk was over capacity. After logging out and in, it says I'm using 4% but the job still won't resume.
Thanks in advance!