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  • netpumber
    Member
    • May 2014
    • 21

    Bam file visualization through console

    Hello!

    The linux server where i working on, hasn't any graphical interface, and i would like to ask, if there is any tool that visualize .bam files through console.

    Thank you.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    samtools tview

    Comment

    • netpumber
      Member
      • May 2014
      • 21

      #3
      Thank you!

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        Does it have X11? So you could use that to export graphical output to your local desktop.

        Comment

        • netpumber
          Member
          • May 2014
          • 21

          #5
          NO it doesn't have X11. Also when i m trying to use the samtools tview returns me that error


          [bam_index_load] fail to load BAM index.
          Cannot read index for 'accepted_hits.bam'

          Comment

          • dpryan
            Devon Ryan
            • Jul 2011
            • 3478

            #6
            Just index the file then (samtools index). You'll need to sort it (samtools sort) if that wasn't already done.

            Comment

            • netpumber
              Member
              • May 2014
              • 21

              #7
              I sorted them, indexed them and when i tried to run tview with .sort.bam file and genome.fa, it returned a huge line only with NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNs.

              Any idea ?

              Comment

              • Richard Finney
                Senior Member
                • Feb 2009
                • 701

                #8
                What are the parameters you used?

                Comment

                • netpumber
                  Member
                  • May 2014
                  • 21

                  #9
                  Results are from tophat2.

                  Code:
                  samtools sort accepted_hints.bam accepted_hints.sort
                  samtools index accepted_hints.sort.bam 
                  samtools tview accepted_hints.sort.bam pathtogenome.fa

                  Comment

                  • dpryan
                    Devon Ryan
                    • Jul 2011
                    • 3478

                    #10
                    You probably want to use the -p option with a position. By default, you start at base 1 of the first contig/chromosome. If there are no alignments there, then you won't see anything except whatever the reference sequence is (if this is for a mammal, then typically a bunch of Ns).

                    Comment

                    • netpumber
                      Member
                      • May 2014
                      • 21

                      #11
                      Ok. Thank you. Seems to work.

                      Comment

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