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  • How convert .gff to .gff3??

    Hi there! I'm trying to convert a simple .gff file to a .gff3 to extract the intergenic sequences of a genome, i was searching for a tool or script to do that but i can find anything :/ little help!
    Regards!

  • #2
    1) Are you sure that you have gff (which is a quite old format) and not gff2/gtf?
    2) Both formats contain start/stop coordinates of genes/exons/transcripts. Why would you want to have gff3 for determining intergenic regions?

    Comment


    • #3
      Answering your questions, here is an example of my gff file:

      scaffold_1 JGI exon 2253 4325 . - . name "estExt_Genemark.C_10001"; transcriptId 143574
      scaffold_1 JGI CDS 2418 4325 . - 0 name "estExt_Genemark.C_10001"; proteinId 143574; exonNumber 1
      scaffold_1 JGI start_codon 4323 4325 . - 0 name "estExt_Genemark.C_10001"
      scaffold_1 JGI stop_codon 2418 2420 . - 0 name "estExt_Genemark.C_10001"
      scaffold_1 JGI exon 5719 7023 . - . name "fgenesh1_pm.1_#_2"; transcriptId 97261
      scaffold_1 JGI CDS 5719 7023 . - 0 name "fgenesh1_pm.1_#_2"; proteinId 97261; exonNumber 2

      There is a program called GFFEX that extract intergenic regions with the fasta and the gff3 faster than other programs.

      Comment


      • #4
        As expected, you're file is in gtf/gff2 format.
        I had a brief look at the program (version 2.2 from http://bioinfo.icgeb.res.in/gff/gffdownloads/) and it is able to handle that format without re-formating anything. Also from looking at the perl scripts, it should be able to handle it - although I'm not sure how it handles "start_codon" / "stop_codon" entries, but "exon", "CDS", "mRNA", etc... are covered.
        What was the (error) message you got when you tried to run the program?

        Comment


        • #5
          The error message looks like this:

          cat: final1: No such file or directory
          C
          O
          M
          P
          L
          E
          T
          E

          adding description to UPSTREAM/PROMOTER_sequences
          C
          O
          M
          P
          L
          E
          cat: local: No such file or directory
          T
          E


          Processing the Output Files

          1/7 Processes Completed

          2/7 Processes Completed

          3/7 Processes Completed

          4/7 Processes Completed

          5/7 Processes Completed

          6/7 Processes Completed

          All Processes are Completed successfully

          ERROR with the run, no output files generated
          ERROR: bad input files

          ######################################################################
          Thanks for using GFF-Extractor !!!!
          ######################################################################

          i tried to transform the file with gffreader from cufflinks but i obtain the same error message...

          Comment

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