- Open "Raw DNA-Seq data processing" workflow
- Input several FASTQ files (denote the number of files as N)
- Input reference sequence
- Remove all elements after "Align Reads with BWA MEM"
- Run the workflow
Current result: There are N+1 *.sam output files on the file system.
- relates to
-
UGENE-5603 Raw DNA-Seq data processing: one output file on dashboard for several input FASTQ files
- Closed