Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • makost
    Junior Member
    • Jun 2010
    • 5

    #1

    Tophat output - Questions

    Hi,
    I've been using Tophat to align 76bp paired-end data to the human genome.
    I used samtools to convert the .BAM file to .SAM format and when looking at the aligned reads I came across the following questions.
    • I understand that for unstranded libraries (like mine) the use of XS tag for reads aligned over splice junctions is essential for Cufflinks. What I don't understand is why for some reads there are multiple alignments at the same position and their only difference is the XS tag. Look here for an example:

      IL28_5635:5:100:10006:3569 137 chr1 160325534 3 14M105N62M * 0 0 CAGACACTGCCAAGGCCCTGGCAGATGTGGCCACGGTGCTGGGACGTGCTCTGTATGAGCTTGCAGGAGGAACCAA %%%%%%%$%%%%%%%%%%%%%%%%%#%"%%%%%#%%!%$#%$$"#$"$#$""$""#"####$#####""""#"""# NM:i:0 XS:A:- NH:i:2 CC:Z:= CP:i:160325534
      IL28_5635:5:100:10006:3569 137 chr1 160325534 3 14M105N62M * 0 0 CAGACACTGCCAAGGCCCTGGCAGATGTGGCCACGGTGCTGGGACGTGCTCTGTATGAGCTTGCAGGAGGAACCAA %%%%%%%$%%%%%%%%%%%%%%%%%#%"%%%%%#%%!%$#%$$"#$"$#$""$""#"####$#####""""#"""# NM:i:0 XS:A:+ NH:i:2

      When I use the genomeCoverageBed function from BEDtools aren't these reads counted twice? Can this somehow be fixed?
    • Do people filter the Tophat output according to flags or MAPQ qualities?
      I would use the reads that are properly paired (flags:83, 99, 147, 163) or any singletons (flags:73, 89, 137, 153) but I don't understand the use of other flags (i.e. flags: 65, 81, 97, 113, 115, 129, 145, 161, 177, 179). What do they mean and should these be filtered out?
  • ozs2006
    Member
    • May 2010
    • 21

    #2
    I join to your question: Do I need to filter these "bad" flags out, and to trust only the "samtools view -f 2"?
    Thanks in advance

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
      by SEQadmin2



      Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

      Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
      ...
      10-14-2026, 09:55 AM
    • SEQadmin2
      New Genomics Technologies Take Aim at Long-Standing Limits
      by SEQadmin2


      Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

      We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
      ...
      09-28-2026, 10:25 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 11:13 AM
    0 responses
    16 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, Yesterday, 10:48 AM
    0 responses
    16 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    35 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-14-2026, 05:39 AM
    0 responses
    42 views
    0 reactions
    Last Post SEQadmin2  
    Working...