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  • ragowthaman
    Member
    • Nov 2009
    • 12

    #1

    a viewer for RNAseq data

    Hi All,
    We have done a RNAseq and aligned the reads against the genome (there is no introns in here) using bowtie. I also have BAM/SAM output files. I am looking for a viewer to view the alignment.

    I tried MapView. Works good. But, there is no way to display the genome annotation information

    others like signalmap, artemis display only the coverage but not the reads themselves. ANy suggestion. I tried lookseq. I have problem setting that up.

    Gowtham
  • jnfass
    Member
    • Aug 2008
    • 88

    #2
    IGV (integrated genomics viewer, from Broad) will display the read alignments, as well as variant positions (without relying on samtools for variant calling) from a bam file ...

    Comment

    • jnfass
      Member
      • Aug 2008
      • 88

      #3
      ... as well as annotation from bed or other file formats (gff, I think?) ... and it displays coverage at certain zoom levels automatically, and you can run a 'count' tool within 'igvtools' that will give you a file that allows you to view (binned) coverage at all zoom levels.

      Comment

      • mgogol
        Senior Member
        • Mar 2008
        • 197

        #4
        IGV is good. UCSC genome browser will also work directly with BAM files, but it might not be what you're after.

        Comment

        • jnfass
          Member
          • Aug 2008
          • 88

          #5
          re: IGV versus UCSCGB ... with IGV it's a snap to set up and run with your own (non-standard) genome. Also, you can view all "chromosomes" (or scaffolds) of your genome at the same time, lined up .. something you can't do with UCSC unless you specifically create a "fake-o-some" fasta file. On the other hand, UCSCGB has table queries, and can link with Galaxy for complicated feature counting / overlap / etc. analysis ...

          pro's and con's ...

          Comment

          • ragowthaman
            Member
            • Nov 2009
            • 12

            #6
            Hi both,
            Thanks for the quick replies. Does the Broad institute has two such tools? GenomeView and Integrated Genome View. It seems IGV needs some conversions.....while at it, i tried genomeview. It worked too. May be IGV is an improved version of Genomeview.

            I will update how my IGV goes. Thanks again.

            Comment

            • jnfass
              Member
              • Aug 2008
              • 88

              #7
              ... hadn't heard of genomeview. Must be a different group within Broad? In any case, if you try and compare both, please let us (here on the forum) know what you think.

              Comment

              • klaas.vandepoele
                Junior Member
                • Jan 2011
                • 6

                #8
                Reference GenomeView

                fyi, GenomeView is developed by Thomas Abeel (Ghent University, BE / Broad).
                For more info, check http://genomeview.org/

                Comment

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