Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • slny
    Member
    • Mar 2011
    • 54

    #1

    BWA alignment followed by TopHat

    Hi,

    I'm reading the TopHat manual. Looks like I can only use bowtie if I'd like to run TopHat. Can I run sequence alignments with BWA and then use the BWA output to run TopHat?

    Thanks,
    Slny
  • shurjo
    Senior Member
    • Jan 2009
    • 132

    #2
    Simple answer - no. TopHat is linked intrinsically with Bowtie. Running it on BWA output rather than raw sequence data could actually be counterproductive.

    Comment

    • slny
      Member
      • Mar 2011
      • 54

      #3
      If so, how could I align the reads from exon junctions if I use BWA? Any other tool(s) should I choose if I use BWA? Bowtie is not good for pair-end sequence alignment.

      Comment

      • shurjo
        Senior Member
        • Jan 2009
        • 132

        #4
        One way would be to use BWA to align against (the genome +a set of known splice junctions). Even so, TopHat may still be the logical choice as you can align against the same junctions (option -j) as well as any others that are discovered from your data.

        Comment

        • pbluescript
          Senior Member
          • Nov 2009
          • 224

          #5
          slny, BWA followed by Tophat is a nice method for paired RNA reads because BWA works so much better for paired end data. I map with BWA and then get unmapped reads or reads with indels or soft clipping and remap them using Tophat. It works well. I generally get more reads mapping overall, but there is a small decrease in the amount of split reads.

          Comment

          • slny
            Member
            • Mar 2011
            • 54

            #6
            Thanks a lot for all the responses. Very helpful.

            pbluescript, do you use BWA for sequence alignments, and then re-align the unmapped reads with Bowtie followed with TopHat for exon junctions? But Bowtie is not good for pair-end sequencing, so the identification of exon junctions with TopHat will be influenced.

            Comment

            • pbluescript
              Senior Member
              • Nov 2009
              • 224

              #7
              Tophat calls Bowtie, so I don't actually use Bowtie alone for mapping RNA reads. The identification of exon junctions still works well since Tophat finds many split reads.

              Comment

              • slny
                Member
                • Mar 2011
                • 54

                #8
                Thanks a lot for your explanation. If I choose bowtie for sequence alignment, should I run everything in TopHat because it also calls Bowtie? If so, I don't need to run a separate Bowtie before I use TopHat.

                Comment

                • pbluescript
                  Senior Member
                  • Nov 2009
                  • 224

                  #9
                  If you use Tophat, you don't need to run Bowtie first. You need to have both installed, but you will only run Tophat.

                  Comment

                  • slny
                    Member
                    • Mar 2011
                    • 54

                    #10
                    Got it. Thanks a lot!

                    Comment

                    Latest Articles

                    Collapse

                    • SEQadmin2
                      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                      by SEQadmin2



                      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                      Despite this, “CRISPR helped turn genome editing from a specialized technique into
                      ...
                      07-31-2026, 11:01 AM
                    • SEQadmin2
                      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                      by SEQadmin2


                      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                      The systematic characterization of the human proteome has
                      ...
                      07-20-2026, 11:48 AM

                    ad_right_rmr

                    Collapse

                    News

                    Collapse

                    Topics Statistics Last Post
                    Started by SEQadmin2, 08-06-2026, 07:41 AM
                    0 responses
                    15 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 08-03-2026, 10:13 AM
                    0 responses
                    31 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 07-31-2026, 02:55 AM
                    0 responses
                    41 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 07-24-2026, 12:17 PM
                    0 responses
                    26 views
                    0 reactions
                    Last Post SEQadmin2  
                    Working...