Scenario
- Open the "Workflow Designer" tab in the UGENE Application Settings.
- Specify the output workflow folder so that there is no enough space on the disk. The free space should be < 5 GB.
- Load the attached workflow.
- Set "R1_cutadapted.fastq.trimmed.fastq" custom file for "Read FASTQ file with reads1".
- Set "R2_cutadapted.fastq.trimmed.fastq" custom file for "Read FASTQ file with reads2".
- Set "data/samples/FASTA/human_T1.fa" for "Align Reads with BWA MEM".
- Run the workflow.
Expected state:
After 8-12 min (when free memory runs out) an error occurs:Subtask "Filter unpaired reads task" is failed: Writing error
- Find the input FASTQ files on the disk.
Expected state: two input FASTQ files are still on the disk.
Actual state: the FASTQ files were unexpectedly deleted from the disk!