Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Crazy unmapped reads

    I don't know if I am understanding the correct meaning of the reads index in sam files.

    This information is present in the Flags description:

    'Next, we have the cases when only one read in a pair is mapped.
    69 - 0001000101 - First read in pair. This read is unmapped but its mate is mapped.
    133 - 0010000101 - 2nd in pair. Read unmapped but mate is mapped.'

    Soooo, does it means that If I have a read with 133 or 69, its paired read can't be present in the unmapped reads file, ok?
    I am assuming that reads with the same index (in this case "M03092:8:000000000-AG2GN:1:2117:2591:14346") are paired. Am I correct? If I am wrong I understood what happened but I'd like to know what are these lines with same index.

    Following this line of thought (same index, paired reads), why are there so many lines of my unmapped paired reads like this?

    M03092:8:000000000-AG2GN:1:2117:2591:14346 69
    M03092:8:000000000-AG2GN:1:2117:2591:14346 133

    Can anyone explain what's going on with these reads?
    Could the reason be a wrong configuration of TopHat or the Bowtie version specified?

  • #2
    It's a bug in TopHat (all versions); it doesn't set the 0x8 bit ("next segment in the template unmapped") when both reads are unmapped.

    This is one of the issues TopHat-Recondition fixes (https://bmcbioinformatics.biomedcent...859-016-1058-x , https://github.com/cbrueffer/tophat-recondition).

    Comment


    • #3
      Thanks a lot, offspring.
      I will re-run my mapping with this new issue!
      =D

      Comment


      • #4
        No Problem! You don't need to re-run the mapping though. TopHat-Recondition is a post-processor; you just pass it your TopHat output directory and it writes a corrected unmapped file. But maybe that's what you meant

        Comment

        Latest Articles

        Collapse

        • seqadmin
          Essential Discoveries and Tools in Epitranscriptomics
          by seqadmin




          The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
          04-22-2024, 07:01 AM
        • seqadmin
          Current Approaches to Protein Sequencing
          by seqadmin


          Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
          04-04-2024, 04:25 PM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, Yesterday, 11:49 AM
        0 responses
        15 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-24-2024, 08:47 AM
        0 responses
        16 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-11-2024, 12:08 PM
        0 responses
        61 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        60 views
        0 likes
        Last Post seqadmin  
        Working...
        X