I have a problem about Galaxy trim galore tools. When I download data from SRA, Galaxy report the error:
1.8 Cutadapt terminated with exit signal: '256'. Terminating Trim Galore run, please check
I don't know what happened with this tools. The input file is fastqsanger.gz from SRA. Also, when I use Fastq Groomer to convert the fastq data. It is still working for three days, even though the raw data is not big. I am not sure whether it is ok.