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  • elizabeth000
    Member
    • Apr 2015
    • 21

    #1

    Negative interval length in GFF file

    I have been given some GFF files to process, and one of these is throwing an error when I attempt to run it through HTSeq-count:

    Error occured when processing GFF file (line 26 of file ./features/promoter.gff):
    Cannot subset to zero-length interval.
    [Exception type: IndexError, raised in _HTSeq.pyx:348]

    Indeed, on line 26, the start value is higher than the end value for the interval.

    Code:
    C20524	flankbed	promoter	1101	1100	.	-	.	ID=CGI_10000033;
    Has anyone encountered this before?
    Should I trust the quality of this GFF file or is something terribly wrong?
    How would you deal with this problem?

    Thanks in advance...
  • Zaag
    Senior Member
    • Nov 2009
    • 112

    #2
    See if it occurs more often and if it is always on the same strand, if so just turn them around.

    Comment

    • diego diaz
      Member
      • Oct 2013
      • 62

      #3
      Be careful with that GFF, it is weird to have a promoter region with a 1 base long (1100 - 1101)

      Comment

      • elizabeth000
        Member
        • Apr 2015
        • 21

        #4
        There are many such lines, with very short intervals! Yes, I'm very worried.
        Unfortunately I do not know how to make gff files myself. I obtained them from the public resource at this address, where it is explained how they were made:


        Since I am completely unfamiliar with Python, I do not understand how the files were generated.

        Comment

        • diego diaz
          Member
          • Oct 2013
          • 62

          #5
          but what do you have to do? maybe there is an easier way to do it, instead using IGV

          Do you have to analyze an unannotated genome?

          Comment

          • elizabeth000
            Member
            • Apr 2015
            • 21

            #6
            The integrated genomics viewer will not be sufficient for me; I have to perform calculations. The genome has been annotated, and many resources are already available.
            If you think there is something strange in the gff file, perhaps there is a way to clean it up? I have very little experience with sequence data, so I need some experts' advice.

            Comment

            • diego diaz
              Member
              • Oct 2013
              • 62

              #7
              If the genome is annotated then it is probably that it is available in UCSC or Ensembl. In these repositories you could get a lot of curated genomic features, such us, repeat regions, TSSs, coding regions, intron, exons, promoters, etc, in many formats.

              Biomart Ensembl website
              http://www.ensembl.org/biomart/martv...030c1fd8678b01

              UCSC tables

              Comment

              • GenoMax
                Senior Member
                • Feb 2008
                • 7142

                #8
                There is a big different between predicted annotations and ones that are vetted by a human (which is why finishing a genome is so expensive).

                You may want to contact the lab that generated the files (http://faculty.washington.edu/sr320/?page_id=551) and ask them about this discrepancy.

                Comment

                • elizabeth000
                  Member
                  • Apr 2015
                  • 21

                  #9
                  Aha! I found the most recent versions on Ensembl. Thank you for pointing me in the right direction.

                  Comment

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