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  • ykdang
    Junior Member
    • Oct 2011
    • 7

    #1

    How to generate GFF?

    I am working on a fungus call Neurosprora. Previous lab member built a gbrowser (1.70) to visualize the deep-seq data with GFF2 file format. Now I obtain some new deep-seq data and want to load it onto that browser. I heard that he used bowtie to do alignment and convert into gff2, but I cannot find the script to convert. Does anyone have similar script which could share? Or just indicate any tools can do this trick? I am not a perl person and don't think I could learn it in a short while.
  • gringer
    David Eccles (gringer)
    • May 2011
    • 845

    #2
    If you have a BAM file (which bowtie can produce), this tutorial suggests that GBrowse can handle BAM directly:



    You could also have a look at the admin tutorial:

    Comment

    • gringer
      David Eccles (gringer)
      • May 2011
      • 845

      #3
      FWIW, I've just today ended up writing a python script to convert from SAM/BAM files to GFF3 files using pysam. The code may be useful for you if you can't find anything else suitable for your conversion.

      For a bit of context, I broke up genomic contigs into 100bp fragments, naming the sequences <contig>#<start>-<end>, then used bowtie2 to map them to the genome -- that's why I've got the 'read.qname.find' bits in the code. My contigs started with 'v', which bowtie replaced with 'N' for some odd reason, so I had to do a bit of extra fiddling to add the 'v' back in.

      Here's the relevant part of my code which does the SAM->GFF conversion:
      Code:
      samFile = pysam.Samfile(samFileName, "r")
      totalCount = 0
      sys.stderr.write("Getting reads from SAM file...")
      sys.stdout.write("##gff-version 3\n")
      gffWriter = csv.writer(sys.stdout, delimiter = '\t')
      for read in samFile:
          totalCount += 1
          if(read.tid > 0):
              qContig = 'v' + read.qname[1:read.qname.find("#")]
              qContigStart = read.qname[read.qname.find("#")+1:read.qname.find("-")]
              qContigEnd = read.qname[read.qname.find("-")+1:]
              tContig = samFile.getrname(read.tid)
              strand = "-" if read.is_reverse else "+"
              score = "."
              for tag in read.tags:
                  if(tag[0] == "XS"):
                      score = str(tag[1]+1000)
              gffWriter.writerow((qContig,
                                  "sam2gff3-"+os.path.basename(samFileName),
                                  "nucleotide_match", qContigStart, qContigEnd,
                                  score, strand, ".",
                                  "Name=SAM_%s,ID=%s-%s;Target=%s %d %d" %
                                  (tContig, qContig, tContig, tContig,
                                   read.pos, read.aend)))
          if(totalCount % 100000 == 0):
              sys.stderr.write(".")
      Last edited by gringer; 11-02-2011, 12:17 PM. Reason: fixed up GFF3 parsing errors, added Name attribute to avoid contig clashes

      Comment

      • ykdang
        Junior Member
        • Oct 2011
        • 7

        #4
        Thanks a lot, that's could be very useful

        Comment

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