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  • zhanghao
    Member
    • Nov 2015
    • 17

    question about hisat2

    I want to use hisat2. According to the manual, "Use extract_splice_sites.py (in the HISAT2 package) to extract splice sites from a GTF file", I do it as:
    bac@bac-X10DAi:~/hisat2-2.0.0-beta$ python extract_splice_sites.py mus.gtf > s.txt

    the mus.gtf is in the hisat2-2.0.0-beta folder, but the output s.txt is empty!!!

    I do not know where is wrong???
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Are there any other errors? Does mus.gtf have content (i.e. it is not empty)?

    Comment

    • zhanghao
      Member
      • Nov 2015
      • 17

      #3
      Originally posted by GenoMax View Post
      Are there any other errors? Does mus.gtf have content (i.e. it is not empty)?
      You are right, it seems the mus.gtf lack something. I just download this gtf file from ensembl at random. I try other gtf files, they are all ok!

      But I found an another problem. When I run hisat2-build to index the genome, if I add --ss and --exons parameters, it can not finish with an error "illlegal instruction (core dump)". Is this due to insufficient memory? If I don't add these parameters, it is ok.

      Also, I want to know whether adding "--ss" and "--exon" will give us a better result? Is these parameter like -G xx.gtf in tophat? and let the software map reads to transcripts first?

      Comment

      • texy34
        Junior Member
        • Mar 2010
        • 1

        #4
        You have to put the --ss and --exon parameters, and --large-index if needed or desired, after the path to your genome sequence even though the online manual and command line help has them before it. Like this:

        hisat2-build -p 16 Triticum_aestivum.IWGSC1.0+popseq.29.dna.genome.fa --large-index --ss wheat_splice_sites.txt --exon wheat_exons.txt Triticum_aestivum

        Comment

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