Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • zorph
    Member
    • May 2010
    • 40

    #1

    tophat total alignment

    does anyone know how to compute total alignment from TopHat. I have 5 files marked file*****.log and they all have the following format:
    # reads processed: 7069046
    # reads with at least one reported alignment: 710849 (10.06%)
    # reads that failed to align: 6227028 (88.09%)
    # reads with alignments suppressed due to -m: 131169 (1.86%)
    Reported 2269253 alignments to 1 output stream(s)


    my reads were 50bp and Tophat divided these into segment lengths of 25bp.
  • shurjo
    Senior Member
    • Jan 2009
    • 132

    #2
    Originally posted by zorph View Post
    does anyone know how to compute total alignment from TopHat. I have 5 files marked file*****.log and they all have the following format:
    # reads processed: 7069046
    # reads with at least one reported alignment: 710849 (10.06%)
    # reads that failed to align: 6227028 (88.09%)
    # reads with alignments suppressed due to -m: 131169 (1.86%)
    Reported 2269253 alignments to 1 output stream(s)


    my reads were 50bp and Tophat divided these into segment lengths of 25bp.
    It would be useful if you define "total alignment" a bit more precisely.

    Comment

    • zorph
      Member
      • May 2010
      • 40

      #3
      my definition of total alignment are all of the reads that can be aligned to the genome.

      I don't care if they're used to make transfrags in the cufflinks algorithm..

      Comment

      • Thomas Doktor
        Senior Member
        • Apr 2009
        • 105

        #4
        Then you're interested in this line:
        # reads with at least one reported alignment: 710849 (10.06%)

        This is a very low mapping ratio, even for an RNA-seq aligner, are there a lot of bad quality reads? Are you sure you mapped to the right species (e.g. human instead of mouse, as sometimes happens for me...) ?

        Comment

        • zorph
          Member
          • May 2010
          • 40

          #5
          my other 4 file***.log files have much better alignment percentages.

          However, when i add the total amount of reads (from the reads processed line, eg. # reads processed: 7069046) from all 5 files, they go well above the # of reads I input to tophat.

          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
          16 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 08-03-2026, 10:13 AM
          0 responses
          32 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-31-2026, 02:55 AM
          0 responses
          42 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...